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早期类风湿性关节炎足踝功能障碍的步态康复:一项新的步态康复计划(大步向前)的可行性研究

Gait rehabilitation for foot and ankle impairments in early rheumatoid arthritis: a feasibility study of a new gait rehabilitation programme (GREAT Strides).

作者信息

Hendry Gordon J, Bearne Lindsay, Foster Nadine E, Godfrey Emma, Hider Samantha, Jolly Lisa, Mason Helen, McConnachie Alex, McInnes Iain B, Patience Aimie, Sackley Catherine, Sekhon Mandeep, Stanley Bethany, van der Leeden Marike, Williams Anita E, Woodburn Jim, Steultjens Martijn P M

机构信息

School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.

Department of Population Health Sciences, King's College London, London, UK.

出版信息

Pilot Feasibility Stud. 2022 May 30;8(1):115. doi: 10.1186/s40814-022-01061-9.

Abstract

BACKGROUND

Foot impairments in early rheumatoid arthritis are common and lead to progressive deterioration of lower limb function. A gait rehabilitation programme underpinned by psychological techniques to improve adherence, may preserve gait and lower limb function. This study evaluated the feasibility of a novel gait rehabilitation intervention (GREAT Strides) and a future trial.

METHODS

This was a mixed methods feasibility study with embedded qualitative components. People with early (< 2 years) rheumatoid arthritis (RA) and foot pain were eligible. Intervention acceptability was evaluated using a questionnaire. Adherence was evaluated using the Exercise Adherence Rating Scale (EARS). Safety was monitored using case report forms. Participants and therapists were interviewed to explore intervention acceptability. Deductive thematic analysis was applied using the Theoretical Framework of Acceptability. For fidelity, audio recordings of interventions sessions were assessed using the Motivational Interviewing Treatment Integrity (MITI) scale. Measurement properties of four candidate primary outcomes, rates of recruitment, attrition, and data completeness were evaluated.

RESULTS

Thirty-five participants (68.6% female) with median age (inter-quartile range [IQR]) 60.1 [49.4-68.4] years and disease duration 9.1 [4.0-16.2] months), were recruited and 23 (65.7%) completed 12-week follow-up. Intervention acceptability was excellent; 21/23 were confident that it could help and would recommend it; 22/23 indicated it made sense to them. Adherence was good, with a median [IQR] EARS score of 17/24 [12.5-22.5]. One serious adverse event that was unrelated to the study was reported. Twelve participants' and 9 therapists' interviews confirmed intervention acceptability, identified perceptions of benefit, but also highlighted some barriers to completion. Mean MITI scores for relational (4.38) and technical (4.19) aspects of motivational interviewing demonstrated good fidelity. The Foot Function Index disability subscale performed best in terms of theoretical consistency and was deemed most practical.

CONCLUSION

GREAT Strides was viewed as acceptable by patients and therapists, and we observed high intervention fidelity, good patient adherence, and no safety concerns. A future trial to test the additional benefit of GREAT Strides to usual care will benefit from amended eligibility criteria, refinement of the intervention and strategies to ensure higher follow-up rates. The Foot Function Index disability subscale was identified as the primary outcome for the future trial.

TRIAL REGISTRATION

ISRCTN14277030.

摘要

背景

早期类风湿关节炎患者足部功能障碍很常见,并会导致下肢功能逐渐恶化。一项以心理技术为支撑以提高依从性的步态康复计划,可能会维持步态和下肢功能。本研究评估了一种新型步态康复干预措施(大步向前)的可行性以及未来开展试验的可能性。

方法

这是一项包含定性成分的混合方法可行性研究。符合条件的是患有早期(<2年)类风湿关节炎(RA)且有足部疼痛的患者。使用问卷评估干预措施的可接受性。使用运动依从性评定量表(EARS)评估依从性。使用病例报告表监测安全性。对参与者和治疗师进行访谈以探讨干预措施的可接受性。使用可接受性理论框架进行演绎主题分析。为评估干预的保真度,使用动机性访谈治疗完整性(MITI)量表对干预环节的录音进行评估。对四个候选主要结局指标的测量特性、招募率、失访率和数据完整性进行了评估。

结果

招募了35名参与者(68.6%为女性),年龄中位数(四分位间距[IQR])为60.1[49.4 - 68.4]岁,病程为9.1[4.0 - 16.2]个月,23名(65.7%)完成了12周的随访。干预措施的可接受性极佳;23名中有21名确信它会有帮助并会推荐;23名中有22名表示这对他们有意义。依从性良好,EARS评分中位数[IQR]为17/24[12.5 - 22.5]。报告了1例与研究无关的严重不良事件。对12名参与者和9名治疗师的访谈证实了干预措施的可接受性,确定了对益处的认知,但也突出了一些完成干预的障碍。动机性访谈在关系方面(4.38)和技术方面(4.19)的平均MITI评分显示出较高的保真度。足部功能指数残疾子量表在理论一致性方面表现最佳,被认为最具实用性。

结论

患者和治疗师认为大步向前干预措施是可接受的,我们观察到干预保真度高、患者依从性好且无安全问题。未来一项测试大步向前干预措施相对于常规护理的额外益处的试验,将受益于修订后的纳入标准、干预措施的完善以及确保更高随访率的策略。足部功能指数残疾子量表被确定为未来试验的主要结局指标。

试验注册号

ISRCTN14277030。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3134/9150324/d8d59eeb11b9/40814_2022_1061_Fig1_HTML.jpg

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