Comparison of Supervised Rehabilitation and Home Exercise Programs in Subacromial Impingement Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-65
SponsorIzmir Katip Celebi University

About this trial

This randomized controlled trial aims to compare the effectiveness of physiotherapist-supervised rehabilitation and home exercise programs in individuals with subacromial impingement syndrome (SAIS). SAIS is a common musculoskeletal disorder characterized by shoulder pain, reduced range of motion, and functional limitations, negatively affecting quality of life.

Participants diagnosed with SAIS will be randomly assigned to one of three groups: a supervised rehabilitation group, a home exercise group, or a control group. Randomization will be performed using an online randomization tool. Individuals in the supervised rehabilitation group will receive a structured physiotherapy program administered by a physiotherapist, while those in the home exercise group will perform a standardized exercise program at home following initial instruction. Participants in the control group will not receive any intervention during the study period and will be assessed only.

Outcome measures including pain intensity, upper extremity function, range of motion, grip strength, sleep quality, and quality of life will be evaluated at baseline and after the intervention period. The results of this study are expected to provide evidence regarding the comparative effectiveness of supervised and home-based exercise approaches in the management of SAIS.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Voluntary participation in the study

Literate in Turkish

Aged between 30 and 65 years

No visual or hearing impairment

Disqualifiers

Presence of a mental or psychological disorder that may affect study findings

Inadequate cooperation

History of upper extremity fracture within the last 6 months

Presence of cervical neurological symptoms

Trial design

Design model

Parallel

Treatments tested in this trial

  • Supervised Rehabilitation Program

    Behavioral

    A physiotherapist-supervised rehabilitation program including pain management approaches, stretching exercises, range of motion exercises, scapular stabilization exercises, strengthening exercises, and activity modification training administered five days per week for four weeks.

  • Home Exercise Program

    Behavioral

    A structured home exercise program including stretching, range of motion, scapular stabilization, and strengthening exercises performed independently at home for four weeks following an education session.

Treatment groups

63 Participants
are divided into 3 treatment groups
Group A: Supervised RehabilitationExperimental treatment 1 intervention
Group B: Home Exercise ProgramExperimental treatment 1 intervention
Group C: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Pain Intensity

Pain intensity will be assessed using the Visual Analog Scale (0-10 cm) during rest, activity, and night pain. Higher scores indicate greater pain severity.

Time frame
Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)

Secondary outcomes

1

Upper Extremity Function

Upper extremity function will be assessed using the Disabilities of the Arm, Shoulder and Hand Questionnaire-Short Form (DASH-SF; 0-100). Higher scores indicate greater disability.

Time frame
Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
2

Shoulder Range of Motion

Shoulder flexion, extension, abduction, internal rotation, and external rotation range of motion will be measured using a universal goniometer.

Time frame
Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
3

Grip Strength

Grip strength of the affected upper extremity will be assessed using a hand dynamometer.

Time frame
Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
4

Sleep Quality

Sleep quality will be assessed using the Single-Item Sleep Quality Scale (0-10). Higher scores indicate poorer sleep quality.

Time frame
Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)

Other outcomes

Sponsors and contacts

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Izmir Katip Celebi University

Lead sponsor

Kirsehir Ahi Evran Universitesi

Collaborator