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Comparative Effects of Percussion Massage Therapy and Instrument-Assisted Soft Tissue Mobilization as Adjuncts to Conventional Physiotherapy in Subacromial Impingement Syndrome: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This assessor-blinded, three-arm, parallel-group randomized controlled trial will investigate the additional effects of percussion massage therapy and instrument-assisted soft tissue mobilization in individuals with subacromial impingement syndrome. Forty-eight participants aged 40-60 years with clinically and magnetic resonance imaging-confirmed subacromial impingement syndrome will be randomly allocated in a 1:1:1 ratio to conventional physiotherapy, percussion massage therapy plus conventional physiotherapy, or instrument-assisted soft tissue mobilization plus conventional physiotherapy. All groups received a standardized four-week conventional physiotherapy programme. Participants in the percussion massage therapy and instrument-assisted soft tissue mobilization groups additionally received their respective interventions three times per week for four weeks. Outcomes were evaluated at baseline and immediately after the four-week intervention. The primary outcome was shoulder joint position sense during flexion and abduction. Secondary outcomes were shoulder range of motion, resting and activity-related pain, upper-extremity disability, and rotator cuff-related quality of life.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 60
Healthy Volunteers: f
View:

• Men or women aged 40 to 60 years.

• Diagnosis of subacromial impingement syndrome confirmed by clinical examination and -magnetic resonance imaging.

• Positive Neer test.

• Positive Hawkins-Kennedy test.

• Positive painful arc test.

• Shoulder symptoms persisting for at least one month.

• Ability and willingness to participate in the assessment and intervention programme.

• Provision of written informed consent.

Locations
Other Locations
Turkey
Istanbul Medipol University
RECRUITING
Istanbul
Contact Information
Primary
Emre Dansuk, PhD
edansuk@medipol.edu.tr
05377790434
Backup
Burak Menek, PhD
bmenek@medipol.edu.tr
Time Frame
Start Date: 2026-08-10
Estimated Completion Date: 2026-10-20
Participants
Target number of participants: 42
Treatments
Experimental: Percussion Massage Therapy Plus Conventional Physiotherapy
Participants will receive the standardized conventional physiotherapy programme for four weeks and will additionally receive percussion massage therapy three times per week for four weeks.
Experimental: IASTM Plus Conventional Physiotherapy
Participants will receive the standardized conventional physiotherapy programme for four weeks and will additionally receive instrument-assisted soft tissue mobilization three times per week for four weeks.
Active_comparator: Conventional Physiotherapy
Participants will receive a standardized, supervised conventional physiotherapy programme five sessions per week for four weeks.
Related Therapeutic Areas
Sponsors
Leads: Emre DANSUK

This content was sourced from clinicaltrials.gov