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CompletedNCT05525403Updated Apr 24, 2023

The Effects of Fatigue on Exercise-Induced Hypoalgesia During a Dynamic Resistance Exercise

An interventional study of Knee Extension Exercise and Quiet Rest in Healthy, sponsored by University of Central Florida. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-04-24.

Sponsored by University of Central Florida · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The primary purpose of this study is to compare immediate changes in pain sensitivity (pressure pain threshold) during quiet rest, low fatigue exercise, and high fatigue exercise.

Read the detailed description

Participants will attend three sessions. Participants will fill out questionnaires, undergo pain sensitivity testing, and be randomly assigned to complete a high and low fatigue exercise on either the second or third session. During the exercise, participants will complete three sets of a single leg knee extension exercise with weight equivalent to 50% of their 1 repetition maximum until they report either a high or low fatigue level. Immediately before and after each set, the research team will examine immediate changes in sensitivity to pressure (pressure pain threshold).

02

Conditions studied

  • Healthy

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03

In context

Fatigue

1,859 studies on the registry are indexed under Fatigue; 376 are open to participants now.

This study's enrollment of 31 is below the median of 54 across 1,439 interventional studies indexed under Fatigue.

Browse Fatigue studies →

Lead sponsor

University of Central Florida is the lead sponsor of 99 studies on the registry; 40 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Pain-free
  • 18-60 years old
  • Participant can appropriately perform the knee extension exercise (assessed during screening)

Exclusion criteria

Exclusion Criteria:

  • Non-English speaking
  • Regular use of prescription pain medications
  • Current or history of chronic pain condition
  • Currently taking blood-thinning medication
  • Systemic medical condition known to affect sensation, such as uncontrolled diabetes or neurological conditions
  • Any contraindication to the application of ice, such as: uncontrolled hypertension (blood pressure over 140/90 mmHg), cold urticaria, cryoglobulinemia, paroxysmal cold hemoglobinuria, circulatory compromise
  • Known presence of cardiovascular, pulmonary, or metabolic disease
  • Current use of tobacco products
  • Not physically ready to exercise without a medical exam as indicated by the Physical Activity Readiness Questionnaire Plus (PAR-Q+)
  • Surgery, injury, or fracture to the lower back or lower extremity within the past 6 months
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
31 participants (actual)

Study arms

  • Experimental
    Low Fatigue Exercise

    Participants will complete a single leg knee extension exercise with weight until they report a fatigue level = 3/10 on the Borg Rating of Perceived Exertion. Participants will complete three sets.

    Other: Knee Extension Exercise

  • Experimental
    High Fatigue Exercise

    Participants will complete a single leg knee extension exercise with weight until they report a fatigue level = 8/10 on the Borg Rating of Perceived Exertion. Participants will complete three sets.

    Other: Knee Extension Exercise

  • Active comparator
    Quiet Rest

    Participants will rest quietly for two minutes, three sets.

    Other: Quiet Rest

Interventions

  • OtherKnee Extension Exercise

    Participants will be seated in a Steel Flex machine with weight equal to 50% of their 1 repetition maximum added to the machine. Participants will extend the dominant knee until the assigned fatigue level.

  • OtherQuiet Rest

    Participants will sit quietly for two minutes, three times.

06

What researchers measure

Primary outcomes

  1. Change in Pressure Pain Threshold

    A digital pressure algometer will be applied to the quadriceps and upper trapezius for two trials each. Participants are instructed to say "stop" or "pain" so the stimulus can be terminated "when the sensation first transitions from pressure to pain" (pain threshold). Participants will rate the pain experienced during the threshold testing using a 101-point numeric pain rate scale (NPRS) anchored with 0= no pain to 100= the most intense pain sensation imaginable immediately following each testing time.

    Time frame: Change from baseline immediately after exercise

Secondary outcomes

  1. Temporal Summation

    Participants will rate a train of 10 heat pulses using the 101-point numerical pain rating scale

    Time frame: Baseline, pre exercise

  2. Heat Pain Threshold

    A thermode will gradually increase temperature. Participants will state when the sensation first becomes painful.

    Time frame: Baseline, pre exercise

  3. Conditioned Pain Modulation

    Pressure pain threshold after an ice water immersion task will be measured.

    Time frame: Baseline, pre exercise

  4. International Physical Activity Questionnaire Short Form

    This is a self-report measure of physical activity that provides data regarding health-related physical activity.

    Time frame: Baseline, pre exercise

  5. Pittsburgh Sleep Quality Index

    This is a 10-item questionnaire in which individuals respond to statements regarding sleep quality. A higher score indicates a worse sleep quality.

    Time frame: Baseline, pre exercise

  6. Pain Catastrophizing Scale

    This is a 13-item questionnaire in which individuals respond to a statement on a five point scale from 0 to 4. Higher scores indicate higher pain catastrophizing levels.

    Time frame: Baseline, pre exercise

  7. Fear of Pain Questionnaire 9

    This is a 9-item questionnaire in which individuals respond to a statement on a five point scale from 1 to 5. Higher scores indicate higher fear of pain.

    Time frame: Baseline, pre exercise

  8. Pain Anxiety Symptom Scale

    This is a 20-item questionnaire in which individuals respond to a statement on a six point scale from 0 to 5. Higher scores indicate higher pain-related anxiety.

    Time frame: Baseline, pre exercise

  9. Brief Resilience Scale

    This is a 6-item questionnaire in which individuals respond to a statement on a five point scale from 1 to 5. Higher scores indicate greater resilience.

    Time frame: Baseline, pre exercise

  10. Preference for and Tolerance of the Intensity of Exercise Questionnaire

    This is a 16-item questionnaire in which individuals respond to a statement on a five point scale from 1 to 5. Higher scores indicate lower tolerance for the intensity of exercise.

    Time frame: Baseline, pre exercise

Other outcomes

  1. 1-repetition maximum testing

    The amount of weight that can be lifted for 1 repetition

    Time frame: Baseline, pre exercise

07

Study locations

1 site
  • University of Central Florida
    Orlando, Florida 32765, United States
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 Apr 24, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05525403
Lead sponsor
University of Central Florida
Responsible party
Abigail Wilson (Assistant Professor, University of Central Florida) — Principal investigator
First posted
Sep 1, 2022
Start date
Oct 28, 2022
Primary completion
Apr 20, 2023
Completion
Apr 20, 2023
Last update
Apr 24, 2023

Study contacts

Abigail Wilson
principal investigator · University of Central Florida

Oversight

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

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This study is completed, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

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