Pain Perception and Exercise-Induced Hypoalgesia Across Circadian Rhythms

NCT07290465 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2025-12-18

No results posted yet for this study

Summary

The goal of this randomized crossover clinical trial is to investigate whether exercise-induced hypoalgesia (EIH) is influenced by circadian rhythm in healthy adults aged 18-40 years.

The main questions it aims to answer are:

* Does the time of day (morning vs. evening) influence changes in pain perception following exercise?
* Do chronotype, sex, or stimulation site (bony vs. muscular) alter the magnitude of this effect?

Participants will:

* Complete questionnaires
* Undergo quantitative sensory testing
* Attend both morning and evening sessions in randomized crossover order

Conditions

  • Exercise Induced Hypoalgesia
  • Circadian Rhythm
  • Pain Perception
  • Healthy Participants
  • Chronotype
  • Physical Therapy

Interventions

BEHAVIORAL

High-Intensity Functional Training (HIFT)

A 12-minute, instructor-led HIFT protocol delivered via the same video to all participants. After a 5-minute warm-up, participants perform six exercises targeting major muscle groups. The exercises are 4 lunges followed by one push-up, 10 high knees followed by 10 shuffles, burpees, squat jumps, skaters, and plank up-downs. Each exercise is done for 40 seconds then 20 seconds rest. The cycle repeats twice for a total of 12 minutes. Rate of Perceived Exertion (Borg scale) is recorded at baseline, post-warmup, during each rest interval, and immediately post-exercise. A physiotherapist supervises performance, ensures correct technique, and enforces safety and target intensity while motivating and encouraging the participant.

BEHAVIORAL

Supervised Deep Breathing

A 12-minute deep breathing session delivered via a prerecorded audio and supervised by a physiotherapist. The breathing rhythm includes inhaling for 4 seconds and exhaling for 6 seconds for a total 1 minute, followed by 1 minute of normal breathing. This cycle is repeated six times for a total duration of 12 minutes. Participants lie supine in a comfortable position and wear headphones. A self-reported Rate of Perceived Relaxation (RPR, 0-10) is recorded before and after. This serves as a non-exercise control to account for relaxation and attention effects.

Sponsors & Collaborators

  • Medipol University

    lead OTHER

Principal Investigators

  • Gizem Ergezen Şahin, Dr. Assistant Professor · Department of Physiotherapy and Rehabilitation/Istanbul Medipol University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-31
Primary Completion
2026-03-31
Completion
2026-04-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07290465 on ClinicalTrials.gov