CClinicalTrials.gg
Status unknownNCT03700996(COFAKS)Updated Sep 28, 2021

Clinical Outcome Following Arthroscopic Knee Surgery

An observational study in Anterior Cruciate Ligament Injury, sponsored by The University of Texas Health Science Center, Houston. Status unknown at 1 site in United States. Open to participants aged 10 Years to 70 Years. Per ClinicalTrials.gov, last updated 2021-09-28.

Sponsored by The University of Texas Health Science Center, Houston · Observational

The sponsor has not verified this record recently (last verified Sep 2021), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Ages
10 Years to 70 Years
Sex
All
01

Study summary

Purpose: There are no existing data available to guide clinicians in the appropriate rehabilitation progression of patients who have undergone knee arthroscopy. The investigator intends to fill this void by establishing normative recovery curves for patients undergoing knee arthroscopy.

Research Design: Prospective Observational Design Procedures: Patients 10-70 years old will be screened for "standard of care" clinical and functional outcomes to occur at standardized time-points (post-op weeks 1-4, 8, 12, 16, 20 and return to sport/activity) following arthroscopic knee surgery. Recovery curves will be plotted for all outcome variables of interest including; (1) International knee Disability Committee (IKDC) survey, (2) Tampa Kinesiophobia scale, (3) Tegner activity scale, (4) Marx activity scale, (5) Passive knee range of motion/heel-height difference, (6) Balance Error Scoring System (BESS), (7) Quad/Hamstring strength ratios, (8) Y-Balance, (9) Functional Movement Screening, (10) Vail-Sport Test, (11) Landing Error Scoring System (LESS), (12) Hop Testing, and the (13) Sports Metrics Test. Polynomial lines-of-best-fit and 95% confidence intervals will be plotted to provide objective recovery curves for clinical utilization and stratification of patient recovery.

Risks: There are no additional risks to "standard physical therapy practice" for post-surgical patients participating in this study. The investigator will not be using invasive procedures or testing modalities that emit radiation.

Benefits \& Clinical Relevance: This information may offer valuable information to clinicians treating patients following knee arthroscopy by providing objective data for each phase of post-operative recovery. Identifying key landmarks and functional milestones may allow the ability to identify patients who are not meeting clinical expectations and subsequently tailor rehabilitation programs to improve recovery trajectories.

02

Conditions studied

  • Anterior Cruciate Ligament Injury

Keywords

  • ACL
03

In context

Anterior Cruciate Ligament Injuries

512 studies on the registry are indexed under Anterior Cruciate Ligament Injuries; 164 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 92 across 127 observational studies indexed under Anterior Cruciate Ligament Injuries.

Browse Anterior Cruciate Ligament Injuries studies →

Lead sponsor

The University of Texas Health Science Center, Houston is the lead sponsor of 880 studies on the registry; 209 are open to participants now.

Of its 170 completed or terminated interventional studies of FDA-regulated products, 140 (82%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Exclusion Criteria:

  • will be surgical candidates who have elected surgical intervention for internal derangement of the knee.

Inclusion criteria

  • Ages 10-70; undergoing primary knee arthroscopy; \& participating in post-operative physical therapy management.

Exclusion criteria

Exclusion Criteria:

  • Patients will be excluded from the study if they elect to not have knee arthroscopy. Have other orthopedic or medical complications (fractures, deep vein thrombosis,) that would be a contraindication to standard post-operative physical therapy care.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 4

  2. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 5

  3. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 6

  4. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 7

  5. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 8

  6. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 9

  7. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 10

  8. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 11

  9. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 12

  10. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 13

  11. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 14

  12. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 15

  13. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 16

  14. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 17

  15. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 18

  16. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 19

  17. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week 20

  18. International Knee Disability Committee (IKDC) Survey

    Self-Report Outcomes: The International Knee Disability Committee Survey is an 18-item instrument designed to measure pain, symptoms, function and sports activity in patients with a variety of knee conditions. A sum score is calculated and then transformed to a 100-point scale, with 100 indicating no restrictions in daily and sports activities and the absence of symptoms. The overall score will be reported.

    Time frame: Post op week Return to Sport: range 21 weeks to 52 weeks

  19. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 4

  20. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 5

  21. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 6

  22. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 7

  23. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 8

  24. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 9

  25. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 10

  26. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 11

  27. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 12

  28. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 13

  29. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 14

  30. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 15

  31. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 16

  32. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 17

  33. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 18

  34. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 19

  35. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week 20

  36. Marx Scale

    Self-Report Outcomes: MARX focuses on four activity points: running, deceleration, cutting (changes directions while running), and pivoting. The four knee functions are rated on a 5-point scale of frequency and scores added up to a maximum of 16 points with a higher score indicating more frequent participation.

    Time frame: Post op week Return to Sport: range 21 weeks to 52 weeks

  37. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 4

  38. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 5

  39. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 6

  40. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 7

  41. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 8

  42. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 9

  43. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 10

  44. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 11

  45. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 12

  46. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 13

  47. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 14

  48. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 15

  49. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 16

  50. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 17

  51. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 18

  52. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 19

  53. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week 20

  54. Anterior Cruciate Ligament-Return to Sport after Injury (ACL-RSI)

    Self-Report Outcomes: Scale consists of 12 questions regarding the psychological impact of returning to sports in the sports population. The items are scored on a visual analogical scale from 0 to 100. With 100 being the better outcome. The overall score will be reported.

    Time frame: Post op week Return to Sport: range 21 weeks to 52 weeks

  55. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 4

  56. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 5

  57. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 6

  58. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 7

  59. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 8

  60. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 9

  61. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 10

  62. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 11

  63. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 12

  64. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 13

  65. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 14

  66. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 15

  67. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 16

  68. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 17

  69. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 18

  70. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 19

  71. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week 20

  72. Range of Motion

    Clinical Measures: The normal movement of the knee measured in degrees from the center of the knee. The instrument used to take the measurement is called a double-armed goniometer.

    Time frame: Post op week Return to Sport: range 21 weeks to 52 weeks

  73. Y-Balance

    Physical Performance

    Time frame: Post op week 8

  74. Y-Balance

    Physical Performance

    Time frame: Post op week 9

  75. Y-Balance

    Physical Performance

    Time frame: Post op week 10

  76. Y-Balance

    Physical Performance

    Time frame: Post op week 11

  77. Y-Balance

    Physical Performance

    Time frame: Post op week 12

  78. Y-Balance

    Physical Performance

    Time frame: Post op week 13

  79. Y-Balance

    Physical Performance

    Time frame: Post op week 14

  80. Y-Balance

    Physical Performance

    Time frame: Post op week 15

  81. Y-Balance

    Physical Performance

    Time frame: Post op week 16

  82. Y-Balance

    Physical Performance

    Time frame: Post op week 17

  83. Y-Balance

    Physical Performance

    Time frame: Post op week 18

  84. Y-Balance

    Physical Performance

    Time frame: Post op week 19

  85. Y-Balance

    Physical Performance

    Time frame: Post op week 20

  86. Y-Balance

    Physical Performance

    Time frame: Post op week Return to Sport: range 21 weeks to 52 weeks

  87. Single Leg Hop

    Physical Performance

    Time frame: Post op week 8

  88. Single Leg Hop

    Physical Performance

    Time frame: Post op week 9

  89. Single Leg Hop

    Physical Performance

    Time frame: Post op week 10

  90. Single Leg Hop

    Physical Performance

    Time frame: Post op week 11

  91. Single Leg Hop

    Physical Performance

    Time frame: Post op week 12

  92. Single Leg Hop

    Physical Performance

    Time frame: Post op week 13

  93. Single Leg Hop

    Physical Performance

    Time frame: Post op week 14

  94. Single Leg Hop

    Physical Performance

    Time frame: Post op week 15

  95. Single Leg Hop

    Physical Performance

    Time frame: Post op week 16

  96. Single Leg Hop

    Physical Performance

    Time frame: Post op week 17

  97. Single Leg Hop

    Physical Performance

    Time frame: Post op week 18

  98. Single Leg Hop

    Physical Performance

    Time frame: Post op week 19

  99. Single Leg Hop

    Physical Performance

    Time frame: Post op week 20

  100. Single Leg Hop

    Physical Performance

    Time frame: Post op week Return to Sport: range 21 weeks to 52 weeks

07

Study locations

1 of 1 sites recruiting
  • The University of Texas Health Science Center-Houston
    Houston, Texas 77030, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03700996
Lead sponsor
The University of Texas Health Science Center, Houston
Collaborators
Memorial Hermann Hospital
Responsible party
Lane Bailey (Director of Research and Education, The University of Texas Health Science Center, Houston) — Principal investigator
First posted
Oct 9, 2018
Start date
Oct 23, 2014
Primary completion
Dec 23, 2021 (estimated)
Completion
Dec 23, 2021 (estimated)
Last update
Sep 28, 2021

Study contacts

Lane Bailey, PhD, PT
Contact
lane.bailey@memorialhermann.org
Lane Bailey
principal investigator · Memorial Hermann Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

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