The Comparison of Different Passive Warm-Up Methods Prior to Exercise

June 29, 2026 updated by: Sezen Karaborklu Argut, Istanbul University - Cerrahpasa

The Comparison of Different Passive Warm-Up Methods Prior to Exercise on Balance and Jump Performance

This randomized controlled trial aims to investigate the acute effects of two passive warm-up methods-infrared heating and therapeutic massage-on vertical jump, horizontal jump, dynamic balance, static balance, and lower extremity muscle flexibility in healthy adults.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey (Türkiye), 34295
        • Istanbul University-Cerrahpaşa Faculty of Health Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age 18-35 years
  • Healthy young adults
  • No alcohol 12 hours prior to testing
  • No smoking 30 minutes prior to testing

Exclusion Criteria:

  • Active musculoskeletal disorder
  • Orthopedic diagnosis in past 6 months
  • Lower extremity or spinal fracture or surgery within last 2 years
  • Use of any assistive device for gait
  • Intra-articular injections in knee, hip, spine within last 6 months
  • Neurological, vestibular, cardiovascular disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Infrared Group
5 minutes of cycling warm-up 10 minutes of infrared application to dominant quadriceps Infrared applied at 90° angle on bare skin while participant rests in prone position Mechanism: IR-induced deep tissue heating increasing molecular activity and passive warm-up effect
Active Comparator: Massage Group
5 minutes of cycling warm-up 10 minutes of standardized classical massage applied by trained personnel Techniques used: Stroking (effleurage), local stroking, kneading (rolling technique) Massage oil warmed in hands prior to application

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump Height
Time Frame: Baseline (Pre-intervention)
Baseline (Pre-intervention)
Dynamic Balance Composite Score
Time Frame: Baseline (Pre-intervention)

The Y-Balance Test is a dynamic balance assessment tool used to evaluate an individual's ability to maintain postural control while reaching in multiple directions. The participant stands on one leg at the center of a Y-shaped grid and reaches as far as possible with the contralateral leg in three directions: anterior, posteromedial, and posterolateral. The maximum reach distance for each direction is measured in centimeters (cm) and normalized to leg length to reduce inter-individual variability.

Outcome Metrics:

Reach distance (cm) in the anterior, posteromedial, and posterolateral directions Dynamic Balance Composite Score (%) =(Sum of the 3 reach directions / 3 times the limb length * 100)

Baseline (Pre-intervention)
Vertical Jump Height
Time Frame: Day 1 (Post-intervention)
30 minutes later after the intervention at the same day
Day 1 (Post-intervention)
Dynamic Balance Composite Score
Time Frame: Day 1 (Post-intervention)

30 minutes later after the intervention at the same day. The Y-Balance Test is a dynamic balance assessment tool used to evaluate an individual's ability to maintain postural control while reaching in multiple directions. The participant stands on one leg at the center of a Y-shaped grid and reaches as far as possible with the contralateral leg in three directions: anterior, posteromedial, and posterolateral. The maximum reach distance for each direction is measured in centimeters (cm) and normalized to leg length to reduce inter-individual variability.

Outcome Metrics:

Reach distance (cm) in the anterior, posteromedial, and posterolateral directions Dynamic Balance Composite Score (%) =(Sum of the 3 reach directions / 3 times the limb length * 100)

Day 1 (Post-intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sit-and-Reach Test
Time Frame: Baseline (Pre-intervention)
Baseline (Pre-intervention)
Horizontal Jump Distance
Time Frame: Baseline (Pre-intervention)
Baseline (Pre-intervention)
Flamingo Static Balance Test Score
Time Frame: Baseline (Pre-intervention)
A balance beam (50 cm long, 4 cm high, and 3 cm wide) and a stopwatch will use. Participant stands on the balance beam with one leg and bents the free leg backward and grip the back of the foot with the hand on the same side, standing like a flamingo. Participant attempts to maintain this position for as long as possible. The time stops if the raised leg touches the ground, and restarts when balance is regained. The test is scored based on the number of mistakes made within one minute. The more mistakes made, the lower the score.
Baseline (Pre-intervention)
Sit-and-Reach Test
Time Frame: Day 1 (Post-intervention)
30 minutes later after the intervention at the same day
Day 1 (Post-intervention)
Horizontal Jump Distance
Time Frame: Day 1 (Post-intervention)
30 minutes later after the intervention at the same day
Day 1 (Post-intervention)
Flamingo Static Balance Test Score
Time Frame: Day 1 (Post-intervention)
30 minutes later after the intervention at the same day A balance beam (50 cm long, 4 cm high, and 3 cm wide) and a stopwatch will use. Participant stands on the balance beam with one leg and bents the free leg backward and grip the back of the foot with the hand on the same side, standing like a flamingo. Participant attempts to maintain this position for as long as possible. The time stops if the raised leg touches the ground, and restarts when balance is regained. The test is scored based on the number of mistakes made within one minute. The more mistakes made, the lower the score.
Day 1 (Post-intervention)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
the International Physical Activity Questionnaire - Short Form (IPAQ-SF)
Time Frame: Baseline (Pre-intervention)
This measure assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting. The distribution of physical activity levels among participants randomly assigned to groups will be evaluated at baseline. In the event of observed differences between groups, the potential impact on the results will be considered in statistical analyses.
Baseline (Pre-intervention)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 26, 2026

Primary Completion (Actual)

June 25, 2026

Study Completion (Actual)

June 25, 2026

Study Registration Dates

First Submitted

February 26, 2026

First Submitted That Met QC Criteria

March 4, 2026

First Posted (Actual)

March 6, 2026

Study Record Updates

Last Update Posted (Actual)

July 1, 2026

Last Update Submitted That Met QC Criteria

June 29, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Subscribe