The Effects of Intensity on Exercise-Induced Hypoalgesia During a Knee Extension Exercise

Sponsor
University of Central Florida (Other)
Overall Status
Recruiting
CT.gov ID
NCT05561582
Collaborator
(none)
60
1
3
11.6
5.2

Study Details

Study Description

Brief Summary

The primary purpose of this study is to to compare immediate changes in pressure pain threshold at the exercising muscle (quadriceps) and a non-exercising muscle (upper trapezius) during low and high weight knee extension exercise. Participants will attend one session that consists of pain sensitivity testing, completion of pain-related psychological questionnaires, and random assignment to one of three interventions: 1) knee extension exercise with a high weight, 2) knee extension exercise with a low weight, or 3) quiet rest.

Condition or Disease Intervention/Treatment Phase
  • Other: Seated knee extension exercise
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effects of Intensity on Exercise-Induced Hypoalgesia During a Knee Extension Exercise
Actual Study Start Date :
Oct 31, 2022
Anticipated Primary Completion Date :
Oct 20, 2023
Anticipated Study Completion Date :
Oct 20, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: High Intensity Exercise

Participants will complete a knee extension exercise with weight equivalent to 75% of their 1-repetition maximum for 3 sets of 10 repetitions.

Other: Seated knee extension exercise
Participants will be seated in a resistance exercise machine. Weight corresponding to the assigned group will be added to the machine. Participants will extend the dominant knee for 3 sets of 10 repetitions.

Experimental: Low Intensity Exercise

Participants will complete a knee extension exercise with weight equivalent to 30% of their 1-repetition maximum for 3 sets of 10 repetitions.

Other: Seated knee extension exercise
Participants will be seated in a resistance exercise machine. Weight corresponding to the assigned group will be added to the machine. Participants will extend the dominant knee for 3 sets of 10 repetitions.

No Intervention: Quiet Rest

Participants will sit quietly for two minutes, three times.

Outcome Measures

Primary Outcome Measures

  1. Pressure Pain Threshold [Change from baseline to immediately after the exercise]

    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.

Secondary Outcome Measures

  1. Conditioned Pain Modulation [Change from baseline to immediately after the exercise.]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
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:
  • 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, 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Central Florida Orlando Florida United States 32765

Sponsors and Collaborators

  • University of Central Florida

Investigators

  • Principal Investigator: Abigail Wilson, University of Central Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Abigail Wilson, Assistant Professor, University of Central Florida
ClinicalTrials.gov Identifier:
NCT05561582
Other Study ID Numbers:
  • 3
First Posted:
Sep 30, 2022
Last Update Posted:
Nov 15, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Nov 15, 2022