"Comparative Effects of PIR and Static Stretching on Hamstring Flexibility" Post-Isometric Relaxation
NCT ID: NCT07153510
Last Updated: 2025-09-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
NA
54 participants
INTERVENTIONAL
2025-04-01
2025-09-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This randomized controlled trial aims to compare the effects of PIR and Active Static Stretching on hamstring flexibility in healthy university students. Participants will be randomly assigned to either PIR or ASS groups and undergo stretching sessions for a specified duration. Hamstring flexibility will be measured using the Active Knee Extension test before and after the intervention. The findings will provide evidence to guide physiotherapy education and clinical practice on the most effective stretching technique for improving hamstring flexibility.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of PIR and PFS on Pain, ROM, and Disabilty in Tight Hamstring Syndrome
NCT06796491
Comparison of Active Isolated Stretch and Post Isometric Relaxation for Hamstring Flexibility.
NCT04024839
Comparison of Post Isometric Relaxation and Post Facilitation Stretching on Hamstring Muscle Flexibility
NCT05727501
"Effects of Passive Static Stretching of 30 Seconds Versus 60 Seconds on the Hamstring Flexibility in Adults With Hamstring Tightness.
NCT06437613
Neurodynamic Sliding Verses Static Stretching
NCT05076825
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Post-Isometric Relaxation (PIR) is a form of muscle energy technique that utilizes a submaximal isometric contraction of the target muscle followed by a passive stretch, aiming to induce reflex relaxation and elongation of the muscle. Active Static Stretching (ASS) involves actively holding the muscle in a lengthened position for a fixed duration, relying on voluntary control and sustained tension to improve flexibility. While both techniques are clinically relevant, comparative evidence regarding their relative effectiveness in improving hamstring flexibility among young healthy populations, particularly Allied Health Sciences students, remains limited.
This randomized controlled trial is designed to compare the immediate and short-term effects of PIR and ASS on hamstring flexibility. A total of 54 students who meet the inclusion criteria will be randomly allocated to either the PIR group or the ASS group. Each group will undergo a structured stretching protocol for a specified period under supervision. Hamstring flexibility will be evaluated pre- and post-intervention using the Active Knee Extension (AKE) test, a valid and reliable measure of hamstring length.
The results of this study are expected to provide evidence on whether PIR or ASS is more effective for improving hamstring flexibility in this population. Findings will have important implications for physiotherapy education, clinical decision-making, and injury prevention strategies in young adults.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Post-Isometric Relaxation
Participants will undergo Post-Isometric Relaxation technique targeting the hamstring muscles. The technique involves an isometric contraction of the hamstring followed by a passive stretch. Participant will be in supine position; hip at 90° flexion, Isometric contraction of hamstrings for 7 seconds, Followed by 15 seconds of passive stretch, 10 repetitions, 3 times/week for 4 weeks
Post-Isometric Relaxation
Participants will undergo Post-Isometric Relaxation technique targeting the hamstring muscles. The technique involves an isometric contraction of the hamstring followed by a passive stretch. Participant will be in supine position; hip at 90° flexion, Isometric contraction of hamstrings for 7 seconds, Followed by 15 seconds of passive stretch, 10 repetitions, 3 times/week for 4 weeks
Active Static Stretching
Participants will perform Active Static Stretching exercises for the hamstrings, where the stretch is held actively without assistance.Seated long sitting position. Participant actively stretches hamstrings for 30 seconds. 10 repetitions, 3 times/week for 4 weeks
Active Static Stretching
Participants will perform Active Static Stretching exercises for the hamstrings, where the stretch is held actively without assistance.Seated long sitting position. Participant actively stretches hamstrings for 30 seconds. 10 repetitions, 3 times/week for 4 week
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Post-Isometric Relaxation
Participants will undergo Post-Isometric Relaxation technique targeting the hamstring muscles. The technique involves an isometric contraction of the hamstring followed by a passive stretch. Participant will be in supine position; hip at 90° flexion, Isometric contraction of hamstrings for 7 seconds, Followed by 15 seconds of passive stretch, 10 repetitions, 3 times/week for 4 weeks
Active Static Stretching
Participants will perform Active Static Stretching exercises for the hamstrings, where the stretch is held actively without assistance.Seated long sitting position. Participant actively stretches hamstrings for 30 seconds. 10 repetitions, 3 times/week for 4 week
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
25 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Health Sciences Lahore
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Tooba Arif
Dr. Tooba Arif, PT
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Health Sciences
Lahore, Punjab Province, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
UHS/DPS-25/1189
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.