Multicomponent supervised tele-rehabilitation versus home-based self-rehabilitation management after anterior cruciate ligament reconstruction: a study protocol for a randomized controlled trial

被引:0
|
作者
Wang, Kexin [1 ,2 ]
Peng, Linbo [3 ,4 ]
You, Mingke [2 ,3 ,4 ]
Deng, Qian [2 ,3 ,4 ]
Li, Jian [2 ,3 ,4 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Clin Res Management, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Sports Med Ctr, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Orthoped, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Orthoped Res Inst, Chengdu, Peoples R China
来源
关键词
Anterior cruciate ligament; ACL reconstruction; Tele-rehabilitation; FOLLOW-UP; PROGRAMS; RETURN; SPORT;
D O I
10.1186/s13018-024-04871-0
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
IntroductionOur study aims to assess the effectiveness of multicomponent supervised tele-rehabilitation compared to home-based self-rehabilitation management in patients following anterior cruciate ligament reconstruction (ACLR).MethodsThe current study is designed as a single-center, single-blinded, randomized controlled, two-arm trial. Participants will be randomized and allocated at a 1:1 ratio into either a multicomponent supervised tele-rehabilitation group or a home-based self-rehabilitation group. All participants receive uniform preoperative education through the HJT software. Participants in the intervention group undergo multicomponent supervised tele-rehabilitation, while those in the control group follow a home-based self-rehabilitation program. All the participants were assessed and measured for the included outcomes at the outpatient clinic before the procedure, and in 2, 4, 8, 12, and 24 weeks after ACLR by two assessors. The primary outcome was the percentage of patients who achieve a satisfactory active ROM at the 12 weeks following the ACLR. The satisfactory active ROM was also collected at 2, 4, 8, and 24 weeks after ACLR. The secondary outcomes were active and passive range of motion (ROM), pain, muscle strength, and function results.Registration detailsEthical approval has been obtained from the West China Hospital Ethics Committee (approval number 2023-1929, December 2023). The trial has been registered on ClinicalTrials.gov (registration number NCT06232824, January 2024).
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页数:8
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