Not Yet RecruitingNot Applicable

The Effect of Fascial Treatment in Patients With Adhesive Capsulitis

Turkey (Türkiye)36 participantsStarted 2025-09-15

Plain-language summary

Our study is unique in that it utilizes a self-designed fascial mobilization protocol and ultrasonographic evaluation for adhesive capsulitis. Therefore, the aim of our study is to investigate the effects of fascial therapy on pain, normal joint range of motion, proprioception, and fascial architecture in patients diagnosed with adhesive capsulitis.

Who can participate

Age range35 Years – 65 Years

SexALL

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

Inclusion Criteria: * Patients diagnosed with adhesive capsulitis by a specialist, * Patients between the ages of 35 and 60, * Those not diagnosed with cervical disc herniation that could cause other shoulder pathologies, * Those who have not participated in an upper extremity-related physiotherapy program within the last 6 months, * Individuals who volunteer to participate in the study, Exclusion Criteria: * Individuals who have undergone shoulder surgery consistent with any pathology, * Individuals with a neurological history, * Individuals diagnosed with diabetes mellitus (DM)

What they're measuring

Ultrasonographic Measurement

Timeframe: through of the study, average 3 weeks

The pain

Timeframe: through of the study, average 3 weeks

Range of Motion

Timeframe: through of the study, average 3 weeks

Proprioception

Timeframe: through of the study, average 3 weeks

Trial details

NCT IDNCT07163884

SponsorHasan Kalyoncu University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-10-15

Contact for this trial

Tuğba GÖNEN, Asisst. Prof. Dr.

505 090 58 46 tugba.badat@hku.edu.tr

View on ClinicalTrials.gov More Adhesive Capsulitis trials