Effectiveness of manual therapy with pragmatic physiotherapy for rotator cuff-related shoulder pain: a pilot randomized clinical trial.

IF 3.1 Q1 REHABILITATION
Archives of physiotherapy Pub Date : 2026-06-24 eCollection Date: 2026-01-01 DOI:10.33393/aop.2026.3684
Gisela Sole, Ari Samaranayaka, Christina Douglas, Meredith Perry, Ricky Bell, Jean-Sébastien Roy, Jeremy Lewis, Nicola Swain
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Abstract

Introduction: Physiotherapy for rotator cuff-related shoulder pain (RCRSP) typically includes patient education and exercise prescription, with manual therapy used as an adjunct to exercise. This parallel two-arm non-inferiority pilot trial determined the feasibility of a full randomised clinical trial comparing pragmatic physiotherapy with manual therapy (MT Group) to pragmatic physiotherapy without manual therapy (NoMT Group) for RCRSP, and explored preliminary treatment effects on patient-reported outcomes.

Methods: Sixty-eight participants with persistent RCRSP were randomised to MT or NoMT groups, receiving physiotherapy treatments over a 3-month period, with only the MT group receiving manual therapy. Feasibility outcomes were recruitment and retention rates, adherence, and intervention fidelity. Research outcome measures were patient-related outcomes at baseline, 3, and 6-month follow-up.

Results: Of 239 volunteers completing the online screening questionnaire, 108 were physically screened, and 70 (65%) were allocated. After two withdrawals, 33 in the MT group and 35 in the NoMT group completed baseline assessment. Retention, adherence, and fidelity exceeded 80% for both groups. Median treatment sessions were 7 for the MT group and 6 for the NoMT group. In the MT group, glenohumeral joint, thoracic spine, and soft tissue mobilisations were commonly used. Delivery of patient education and exercise prescription was similar between groups. QuickDASH between-group mean differences were below the non-inferiority margin. Self-efficacy favoured the MT group at 6-month follow-up.

Conclusion: Results support feasibility for a full trial. Strategies to improve participant diversity are required. Definitive outcomes require confirmation in a full trial.

手工治疗与实用物理治疗肩袖相关肩痛的有效性:一项随机临床试验。
简介:肩袖相关性肩痛(RCRSP)的物理治疗通常包括患者教育和运动处方,手工治疗作为运动的辅助手段。这项平行的两臂非效性试验确定了一项完全随机临床试验的可行性,该试验比较了实用物理治疗加手工治疗(MT组)和实用物理治疗不加手工治疗(NoMT组)治疗RCRSP的可行性,并探讨了初步治疗效果对患者报告结果的影响。方法:68名持续性RCRSP患者被随机分为MT组或NoMT组,在3个月的时间内接受物理治疗,只有MT组接受手工治疗。可行性结果包括招募率、留任率、依从性和干预保真度。研究结果测量为基线、3个月和6个月随访时的患者相关结果。结果:239名完成在线筛查问卷的志愿者中,有108人接受了物理筛查,70人(65%)被分配。两次停药后,MT组33例,NoMT组35例完成基线评估。两组患者的保留率、依从性和忠诚度均超过80%。MT组中位疗程为7次,NoMT组中位疗程为6次。MT组常用肩关节、胸椎和软组织活动。患者教育和运动处方的提供在两组之间相似。QuickDASH组间平均差异低于非劣效性边界。在6个月的随访中,自我效能感倾向于MT组。结论:结果支持全面试验的可行性。需要提高参与者多样性的战略。最终结果需要在全面试验中得到确认。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.60
自引率
0.00%
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审稿时长
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