Department of Education and Psychology, Health Psychology Division, Freie Universität Berlin, Habelschwerdter Allee 45, Berlin, 14195, Germany.
Centre for Muscle- and Bone Research, Department of Radiology, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, Berlin, 12200, Germany.
BMC Musculoskelet Disord. 2023 Jul 4;24(1):550. doi: 10.1186/s12891-023-06661-x.
This primary analysis evaluated the "PREVenting the impairment of primary Osteoarthritis by high-impact long-term Physical exercise regimen-Psychological Adherence Program" (PrevOP-PAP), designed to support patients with osteoarthritis of the knee (OAK) to engage in regular moderate-to-vigorous physical activity (MVPA) to reduce OAK symptoms (WOMAC scores). Theory-based on the health action process approach (HAPA), the intervention targeted volitional precursors of MVPA change: action and coping planning, maintenance and recovery self-efficacy, action control, and social network formation. We hypothesized that compared to an active control condition, increases in MVPA at the end of the 12-month intervention would translate into lower WOMAC scores at 24 months in the intervention condition.
Participants with radiographically verified moderate OAK (N = 241; 62.66% female; M(SD) = 65.60(7.61) years) were randomly assigned to the intervention (51%) or the active control condition. WOMAC scores (24 months) were the primary -, accelerometer-assessed MVPA (12 months) the key secondary outcomes. The PrevOP-PAP was a 12-month intervention with computer-assisted face-to-face and phone-based sessions designed to increase HAPA-proposed volitional precursors of MVPA change (up to 24 months; secondary outcomes). Intent-to-treat analyses included multiple regression and manifest path models.
MVPA (12 months) did not mediate effects of the PrevOP-PAP on WOMAC scores (24 months). Compared to the active control condition, WOMAC scores (24 months) were lower in the intervention condition, but this effect did not remain stable in sensitivity analyses (b(SE) = -8.41(4.66), 95%-CI [-17.53; 0.71]). However, exploratory analyses revealed significantly stronger reductions in WOMAC-pain (24 months) in the intervention condition (b(SE) = -2.99(1.18), 95%-CI [-5.36; -0.63]). Groups did not differ in MVPA at 12 months (b(SE) = -3.78(3.42), 95%-CI [-10.80; 2.58]). Of the proposed precursors of MVPA change, action planning was higher in the intervention than in the control condition (24 months; b(SE) = 0.64(0.26), 95%-CI [0.14; 1.15]).
Compared to an active control condition, the PrevOP-PAP did not produce reliable effects on WOMAC scores and none on preceding MVPA. Of the HAPA-proposed volitional precursors, only action planning was sustainably increased. Future interventions should use m-health applications to digitally support long-term changes in proposed volitional precursors of MVPA change.
German Clinical Trials Register; https://drks.de/search/de/trial/DRKS00009677 ; also available at http://apps.who.int/trialsearch/ ; registration number: DRKS00009677; date of registration: 26/01/2016.
本主要分析评估了“通过高冲击长期体育锻炼方案-心理坚持计划预防原发性骨关节炎损害”(PrevOP-PAP),旨在支持膝骨关节炎(OAK)患者进行规律的中等至剧烈体力活动(MVPA),以减轻 OAK 症状(WOMAC 评分)。该干预措施基于健康行动过程方法(HAPA)理论,针对 MVPA 变化的意志前体:行动和应对计划、维持和恢复自我效能、行动控制和社交网络形成。我们假设,与积极对照条件相比,12 个月干预结束时 MVPA 的增加将转化为干预条件下 24 个月时 WOMAC 评分的降低。
参与者为影像学证实的中度 OAK(N=241;62.66%为女性;M(SD)=65.60(7.61)岁),随机分配到干预组(51%)或积极对照条件。WOMAC 评分(24 个月)为主要结局,加速度计评估的 MVPA(12 个月)为关键次要结局。PrevOP-PAP 是一项为期 12 个月的干预措施,包括计算机辅助面对面和电话会议,旨在增加 HAPA 提出的 MVPA 变化的意志前体(最多 24 个月;次要结局)。意向治疗分析包括多元回归和显式路径模型。
MVPA(12 个月)并未介导 PrevOP-PAP 对 WOMAC 评分(24 个月)的影响。与积极对照条件相比,干预组的 WOMAC 评分(24 个月)较低,但在敏感性分析中这种影响并不稳定(b(SE)=-8.41(4.66),95%CI [-17.53;0.71])。然而,探索性分析显示,干预组 WOMAC 疼痛(24 个月)明显降低(b(SE)=-2.99(1.18),95%CI [-5.36;-0.63])。两组在 12 个月时的 MVPA 无差异(b(SE)=-3.78(3.42),95%CI [-10.80;2.58])。在 MVPA 变化的提议前体中,行动规划在干预组中高于对照组(24 个月;b(SE)=0.64(0.26),95%CI [0.14;1.15])。
与积极对照条件相比,PrevOP-PAP 对 WOMAC 评分和之前的 MVPA 均无可靠影响。在 HAPA 提出的意志前体中,只有行动规划得到了持续的提高。未来的干预措施应使用移动健康应用程序,以数字方式支持 MVPA 变化的提议意志前体的长期变化。
德国临床试验注册处;https://drks.de/search/de/trial/DRKS00009677;也可在 http://apps.who.int/trialsearch/ 获得;注册号:DRKS00009677;注册日期:2016 年 1 月 26 日。