Evaluation of Pain, Upper Extremity Function, and Social Appearance Anxiety in Adults With Obstetric Brachial Plexus Palsy Who Underwent Shoulder Tendon Transfer Surgery
Recruiting · NCT07655271 · Observational (researchers observe without assigning treatment) · Lead sponsor:
Biruni University
View the official record on ClinicalTrials.gov →
Interventions studied
Clinical Assessment Battery
What this trial is about
This observational study aims to evaluate pain and upper extremity function in adults with obstetric brachial plexus palsy who underwent shoulder tendon transfer surgery using the Modified Hoffer technique during childhood. Data on the long-term clinical outcomes of this surgical procedure in adulthood are limited. Participants with obstetric brachial plexus palsy and healthy age-matched individuals will be assessed in a single session. The evaluations will include pain, range of motion, muscle strength, upper extremity functional status, social appearance anxiety, and role performance. The study aims to describe the clinical profile of adults with obstetric brachial plexus palsy after Modified Hoffer tendon transfer and compare their outcomes with healthy peers.
Who can take part
Age range
18 Years to 40 Years
Healthy volunteers
Yes - healthy volunteers may be accepted
Study type
Observational (researchers observe without assigning treatment)
Eligibility criteria (as published)
Inclusion and Exclusion Criteria
Inclusion Criteria for Individuals With Brachial Plexus Birth Palsy:
* Being between 18 and 40 years of age.
* Having a diagnosis of unilateral brachial plexus birth palsy.
* Having undergone shoulder tendon transfer surgery using the Modified Hoffer Technique.
* Having at least 5 years elapsed since the last surgery.
* Having a cognitive and communication level sufficient to comply with the assessment process.
* Agreeing to participate voluntarily in the study and signing the informed consent form.
Inclusion Criteria for Healthy Individuals:
* Being between 18 and 40 years of age.
* Having no history of upper extremity-related surgery within the last 5 years.
* Having a cognitive and communication level sufficient to comply with the assessment process.
* Agreeing to participate voluntarily in the study and signing the informed consent form.
Exclusion Criteria for All Participants:
* Having a neurological disease.
* Having another orthopedic problem or a history of trauma in the affected upper extremity.
* Having a history of systemic disease requiring an acute attack or hospitalization within the last 3 months.
* Pregnancy or being less than 6 months postpartum.
Where it is running
1 location listed.
Read the full protocol, contacts and eligibility on ClinicalTrials.gov →