ClinicalTrials.gg
RecruitingNCT07815340Updated Sep 29, 2026

Effects Of Criteria Versus Time-Based Rehabilitation On Return To Play In Football Players

An interventional study of Experimental: Criteria based and Active comparator: Time based rehabilitation in Hamstring Muscle Strain, sponsored by Riphah International University. Recruiting at 2 sites in Pakistan. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-09-29.

Sponsored by Riphah International University · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Sep 2026; still recruiting 1 month later.
Updated Sep 29, 2026Now RecruitingSite recruiting status changedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This randomized controlled trial compares criteria-based rehabilitation (CBR) with time-based rehabilitation (TBR) for football players aged 18-35 with ACL reconstruction, hamstring strain, or ankle sprain. Both groups receive a six-week supervised rehabilitation program; the progression rules differ between groups.

Read the detailed description

Eligible football players will be recruited from local football clubs and academies in Islamabad Capital Territory and Rawalpindi. Written informed consent will be obtained. Participants will be randomly allocated 1:1 using a concealed, computer-generated sequence. Baseline demographic, functional, and psychological measures will be collected. Both groups follow the same general phase-based rehabilitation structure under licensed physiotherapist supervision. CBR progression depends on objective functional and psychological milestones; TBR progression follows fixed time intervals and return-to-play clearance at week 6 irrespective of milestones. Progression is paused or regressed if pain is ≥4/10 on VAS or swelling returns.

02

Conditions studied

  • Hamstring Muscle Strain

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Keywords

  • ankle sprain
  • reinjury
  • reactive strength
03

In context

Ankle Injuries

350 studies on the registry are indexed under Ankle Injuries; 74 are open to participants now.

This study's planned enrollment of 52 is close to the median of 54 across 270 interventional studies indexed under Ankle Injuries.

Browse Ankle Injuries studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,193 studies on the registry; 650 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Injury Type: ACL reconstruction, hamstring strain, and ankle sprain.
  • Rehabilitation Phase: Phase 3 for ACL injuries, Phase 1\&2 for hamstring strains and ankle sprains.
  • Football Activity: Active at club or regional football level

Exclusion criteria

Exclusion Criteria:

  • History of Major surgery in affected limb
  • Chronic neurological or musculoskeletal disorder
  • Non-football athletes
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
52 participants (estimated)

Study arms

  • Experimental
    Criteria based rehabilitation

    Participants in this group will undergo a 6-week criteria-based rehabilitation program,consisting of 3-5 supervised sessions per week, each lasting 45-60 minutes. Exercise intensity will be progressively increased from low (40-50% of maximum effort) during early phases to high intensity (70-85%) in later stages, depending on individual performance and pain tolerance. Progression will depend on achieving specific functional and psychological benchmarks rather than elapsed time.

    Other: Experimental: Criteria based

  • Active comparator
    Time based rehabilitation

    Participants in this group will follow a fixed 6-week time-based program with 3-5 sessions per week (45-60 minutes/session). Exercise intensity will progress automatically from low to high each week, regardless of functional test results.

    Other: Active comparator: Time based rehabilitation

Interventions

  • OtherExperimental: Criteria based

    * Weeks 1-2: Focus on pain control, ROM restoration, and isometric strengthening (low intensity, 3-4 sets of 10-15 reps). * Weeks 2-4: Closed-chain and eccentric strengthening (moderate intensity, 3 sets of 12-15 reps), balance training, and jogging once LSI ≥ 80%. * Weeks 4-6: Plyometrics, agility, sprinting, and football-specific drills (high intensity, 4-5 sets, 80-85% effort). Participants will only progress or return to play upon meeting the criteria: hop test LSI ≥ 90%, SEBT symmetry, improved ACLRSI,

  • OtherActive comparator: Time based rehabilitation

    Weeks 1-2: Pain reduction and early strengthening (low intensity, 3 sets of 10-12 reps). * Weeks 2-4: General strengthening, proprioception, and jogging (moderate intensity, 3 sets of 12-15 reps). * Weeks 4-6: Plyometrics, agility, sprinting, and football-specific drills (high intensity, 70-85% effort) All participants will be cleared for return to play at the end of Week 6, regardless of whether they have achieved functional or psychological milestones, reflecting a traditional time-driven rehabilitation approach. This design reflects conventional rehabilitation models used in previous comparative studies, in which exercise progression and RTP clearance are determined by elapsed time rather than by functional recovery.

06

What researchers measure

Primary outcomes

  1. Hop battery test (single, triple, and crossover hop) including limb symmetry index (LSI)

    A tool to assess lower-limb strength, power, symmetry and functional performance in athletes post-injury; demonstrates good test-retest reliability (ICC ≈ 0.85-0.97) and valid discriminatory ability, though its capacity to predict re-injury remains inconsistent. Depends on individual hop test; usually reported as distance. Higher distance generally indicates better performance

    Time frame: At baseline, 0 weeks 6 weeks post-intervention

  2. Star Excursion Balance Test (SEBT)

    Evaluates dynamic balance and postural control; high reliability (ICC 0.85-0.91) and validated in athletes. no fixed universal minimum/maximum; reach distance is recorded in cm and may be normalized to limb length as a percentage Higher reach distance/normalized score = better dynamic postural balance

    Time frame: At Baseline After 6 weeks

  3. Anterior Cruciate Ligament -RSI (Return to Sport after Injury Scale)

    Measures psychological readiness and fear of re-injury; strong internal consistency (α = 0.94) and test-retest reliability (ICC = 0.90) 0-100 Higher score = greater psychological readiness to return to sport

    Time frame: At baseline After 6 weeks of intervention

  4. Tampa Scale of Kinesiophobia (TSK)

    Assesses fear of movement and re-injury; validated in musculoskeletal populations with good internal consistency (α = 0.810.87) and test-retest reliability (ICC = 0.84-0.90) 17-68 for the 17-item version Higher score = greater fear of movement/reinjury

    Time frame: at baseline at 6 weeks post intervention

  5. Landing Error Scoring System (LESS)

    The LESS is a movement screen used to identify specific movement patterns of the lower extremities that may increase an individual's risk for noncontact ACL injury. 0-17 Lower score = better landing technique; higher score = more landing errors

    Time frame: at baseline at 6 weeks post intervention

  6. Reactive Strength Index (RSI)

    Measures reactive strength and stretch-shortening cycle efficiency; demonstrates good test-retest reliability (ICC = 0.87) in athletes. No fixed minimum/maximum; calculated as jump height ÷ ground contact time Higher value = better reactive strength/stretch-shortening-cycle performance

    Time frame: at baseline 6 weeks post intervention

  7. One-Repetition Maximum (1RM)

    This tool is used to assess the strength of the athlete objectively. No universal fixed minimum/maximum; expressed as the maximum load lifted once, usually in kg Higher value = greater muscular strength

    Time frame: at baseline 6 weeks post intervention

  8. Y-Balance Test (YBT)

    The Y Balance Test is a functional screening tool used to assess dynamic balance, core stability, and injury risk in athletes and patients Composite score: 0-100%; individual reach distances are also recorded Higher score = better dynamic balance

    Time frame: at baseline 6 weeks post intervention

07

Study locations

2 of 2 sites recruiting
  • Mescon Islamabad football academy
    Islamabad, Federal 051, Pakistan
    Recruiting
  • Mescon Islamabad Football Academy (MIFA)
    Islamabad, Pakistan
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Sep 2026 (actual). Primary completion is estimated for Dec 2026, 3 months after the start.

Of 138 non-industry interventional studies with no phase under Ankle Injuries, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 30. This study's planned 3 months is below that.

Counting every sponsor, half of 141 studies reached it within 9 months; a quarter within 4 and three quarters within 31.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 6, 2026
First posted
Sep 11, 2026
StartActual
Sep 25, 2026
Primary completionEst.
Dec 25, 2026
CompletionEst.
Jan 5, 2027
Last update
Sep 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Not yet recruiting→Recruiting
changed Sep 29, 2026
Sites
2 sites changed recruiting status (2 now recruiting)
Show 2 sites
  • Mescon Islamabad football academy · Islamabad, Pakistanno status→Recruiting
  • Mescon Islamabad Football Academy (MIFA) · Islamabad, Pakistanno status→Recruiting
Sep 29, 2026
Show all 1 update
  1. Sep 29, 2026
    Not yet recruiting→Recruiting
    2 sites changed recruiting status (2 now recruiting)
    Show 2 sites
    • Mescon Islamabad football academy · Islamabad, Pakistanno status→Recruiting
    • Mescon Islamabad Football Academy (MIFA) · Islamabad, Pakistanno status→Recruiting
    + 1 other change: date precision

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07815340
Responsible party
Sponsor
First posted
Sep 11, 2026
Start date
Sep 25, 2026
Primary completion
Dec 25, 2026 (estimated)
Completion
Jan 5, 2027 (estimated)
Last update
Sep 29, 2026

Study contacts

Saadia Batool
Contact
saadia.batool@riphah.edu.pk
03165131870
rida zafar
Contact
rida.zafar@riphah.edu.pk
03368753273
Ramsha Ali
principal investigator · Riphah International University

Oversight

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

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