Not Yet RecruitingNot Applicable

Effect of Myofascial Release on Pain, Grip Strength, Manual Dexterity, and Quality of Life in Late-Term Rehabilitation of Hand Flexor Tendon Repairs

Turkey (Türkiye)42 participantsStarted 2025-11-30

Plain-language summary

The aim of this study was to investigate the effectiveness of myofascial release exercises performed in the late period compared to classical physiotherapy training in individuals with hand flexor tendon repair.

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Being between the ages of 18 and 65, * Having a hand flexor tendon injury and subsequent surgery, * Not having a symptom of deterioration in the extremity being cared for, * Having adequate communication skills, * Voluntarily participating in the study. Exclusion Criteria: * Having had previous hand surgery for any reason other than this injury, * Having a comorbid mental, physical, or neurological chronic illness, * Having cognitive problems that prevent communication, * Having any problem that prevents cooperation.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

The pain

Timeframe: through of the study, average 8 weeks

Grip strength

Timeframe: through of the study, average 8 weeks

Hand skills

Timeframe: through of the study, average 8 weeks

Short form SF-36 Quality of life

Timeframe: through of the study, average 8 weeks

Trial details

NCT IDNCT07233369

SponsorHasan Kalyoncu University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-01-30

Contact for this trial

Tuğba Çevik, PT

05345251455 cvktubaa@gmail.com

View on ClinicalTrials.gov More Hand Flexor Tendon trials

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.