Comparison of Supervised Rehabilitation and Home Exercise Programs in Subacromial Impingement Syndrome (SAIS-REHAB)
Comparison of the Effectiveness of a Physiotherapist-Supervised Rehabilitation Program and Home Exercise Education in Subacromial Impingement Syndrome
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.
調査の概要
詳細な説明
Subacromial impingement syndrome (SAIS) is one of the most common causes of shoulder pain, leading to decreased range of motion, muscle weakness, functional limitations, and reduced quality of life. Exercise-based rehabilitation is considered a primary conservative treatment approach. However, access to supervised physiotherapy services may be limited due to long waiting times and healthcare system constraints. Home exercise programs may serve as an alternative, but evidence comparing their effectiveness with supervised rehabilitation remains limited.
This study is designed as a randomized controlled trial to compare the effectiveness of physiotherapist-supervised rehabilitation and home exercise programs in individuals with SAIS. A total of 63 participants who meet the inclusion criteria will be recruited and randomly assigned into three groups: supervised rehabilitation, home exercise, and control.
Randomization will be performed using an online randomization tool. Participants allocated to the supervised rehabilitation group will receive a structured rehabilitation program consisting of pain management modalities, range of motion exercises, strengthening exercises, and functional training under the supervision of a physiotherapist, five days per week for four weeks. The home exercise group will receive a structured exercise program including stretching, strengthening, and mobility exercises after a single training session and will continue the program independently at home. Participants in the control group will not receive any intervention during the study period and will be included in the supervised rehabilitation program after the final assessment.
Outcome measures will include pain intensity assessed by Visual Analog Scale, upper extremity function assessed by the Disabilities of the Arm, Shoulder and Hand questionnaire (DASH), shoulder range of motion measured by goniometer, grip strength measured by dynamometer, sleep quality assessed by a single-item sleep quality scale, and quality of life assessed by the WHOQOL-BREF. Assessments will be conducted at baseline and at the end of the 4-week intervention period.
The findings of this study will contribute to the literature by providing evidence on the comparative effectiveness of supervised rehabilitation and home-based exercise programs and may guide clinical decision-making in the management of SAIS.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究場所
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Kırşehir
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Kırşehir、Kırşehir、トルコ（Türkiye）、40100
- 募集
- Kırşehir Ahi Evran University
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コンタクト：
- Atahan Turhan, PhD
- 電話番号：90 386 280 40 81 - 4107 - 4070
- メール：atahanturhan@hotmail.com
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Voluntary participation in the study
- Literate in Turkish
- Aged between 30 and 65 years
- No visual or hearing impairment
- Diagnosed with unilateral subacromial impingement syndrome by a specialist physician
- Positive painful arc test, Infraspinatus test, and Hawkins-Kennedy test
- Pain during overhead activities
Exclusion Criteria:
- 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
- Glenohumeral instability
- Acromioclavicular joint pathology
- Full-thickness rotator cuff tear or total rupture
- Signs of glenohumeral osteoarthritis
- History of frozen shoulder
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：Supervised Rehabilitation
Participants in this group will receive a physiotherapist-supervised rehabilitation program five days per week for four weeks.
The program will include pain management approaches, stretching exercises, range of motion exercises, scapular stabilization exercises, strengthening exercises, and activity modification training according to standard physiotherapy procedures.
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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.
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実験的：Home Exercise Program
Participants in this group will receive a structured home exercise program after an education session.
The program will include stretching, range of motion, scapular stabilization, and strengthening exercises to be performed independently at home for four weeks.
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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.
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介入なし：Control
Participants in this group will not receive any intervention during the four-week study period.
Baseline and follow-up assessments will be performed.
Individuals who are required to wait more than four weeks before starting physiotherapy sessions will be included in this group.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Pain Intensity
時間枠：Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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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.
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Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Upper Extremity Function
時間枠：Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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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.
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Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Shoulder Range of Motion
時間枠：Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Shoulder flexion, extension, abduction, internal rotation, and external rotation range of motion will be measured using a universal goniometer.
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Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Grip Strength
時間枠：Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Grip strength of the affected upper extremity will be assessed using a hand dynamometer.
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Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Sleep Quality
時間枠：Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Sleep quality will be assessed using the Single-Item Sleep Quality Scale (0-10).
Higher scores indicate poorer sleep quality.
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Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Quality of Life-WHOQOL-BREF
時間枠：Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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Quality of life will be assessed using the WHOQOL-BREF questionnaire.
Higher scores indicate better quality of life
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Baseline (Day 0, prior to intervention) and Week 4 (end of intervention)
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協力者と研究者
出版物と役立つリンク
一般刊行物
- Gutierrez-Espinoza H, Araya-Quintanilla F, Cereceda-Muriel C, Alvarez-Bueno C, Martinez-Vizcaino V, Cavero-Redondo I. Effect of supervised physiotherapy versus home exercise program in patients with subacromial impingement syndrome: A systematic review and meta-analysis. Phys Ther Sport. 2020 Jan;41:34-42. doi: 10.1016/j.ptsp.2019.11.003. Epub 2019 Nov 6.
- Diercks R, Bron C, Dorrestijn O, Meskers C, Naber R, de Ruiter T, Willems J, Winters J, van der Woude HJ; Dutch Orthopaedic Association. Guideline for diagnosis and treatment of subacromial pain syndrome: a multidisciplinary review by the Dutch Orthopaedic Association. Acta Orthop. 2014 Jun;85(3):314-22. doi: 10.3109/17453674.2014.920991. Epub 2014 May 21.
- Horowitz EH, Aibinder WR. Shoulder Impingement Syndrome. Phys Med Rehabil Clin N Am. 2023 May;34(2):311-334. doi: 10.1016/j.pmr.2022.12.001. Epub 2023 Feb 26.
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 2520
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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