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基于社交媒体的干预(Run4Love)对 HIV 感染者抑郁症状的长期影响:一项随机对照试验的 3 年随访。

Long-term Effects of a Social Media-Based Intervention (Run4Love) on Depressive Symptoms of People Living With HIV: 3-Year Follow-up of a Randomized Controlled Trial.

机构信息

Department of Medical Statistics, School of Public Health, Sun Yat-sen University, Guangzhou, China.

Department of Population and Quantitative Health Sciences, University of Massachusetts Chan Medical School, Worcester, MA, United States.

出版信息

J Med Internet Res. 2022 Jun 28;24(6):e36809. doi: 10.2196/36809.

Abstract

BACKGROUND

Emerging studies have shown the effectiveness of mobile health (mHealth) interventions in reducing depressive symptoms among people living with HIV. Most of these studies included only short-term follow-up, with limited data on long-term effects.

OBJECTIVE

The purpose of this study is to assess the long-term effects of a randomized controlled trial called Run4Love on depressive symptoms among people living with HIV at 1-year and 3-year follow-ups.

METHODS

A total of 300 people living with HIV with depressive symptoms were recruited and randomized to an intervention or a control group in Guangzhou, China, from September 2017 to January 2018. The intervention group received a 3-month Run4Love program, including adapted evidence-based cognitive behavioral stress management courses and exercise promotion via WeChat (Tencent), a popular social media app. The control group received usual care and a brochure on nutrition. The primary outcome was reduction in depressive symptoms, measured using the Center for Epidemiological Studies-Depression (CES-D) scale. Data used in this study were collected at baseline and at the 1-year and 3-year follow-ups. Generalized estimating equations were used to examine the group differences at 1-year and 3-year follow-ups.

RESULTS

Approximately half of the participants completed the assessment at 1-year (149/300, 49.7%) and 3-year (177/300, 59%) follow-ups. At 1-year follow-up, participants in the intervention group reported significant reduction in depressive symptoms compared with the control group (CES-D: from 23.9 to 18.1 in the intervention group vs from 24.3 to 23.3 in the control group; mean -4.79, SD 13.56; 95% CI -7.78 to -1.81; P=.002). At 3-year follow-up, between-group difference in CES-D remained statistically significant (from 23.9 to 20.5 in the intervention group vs from 24.3 to 24.4 in the control group; mean -3.63, SD 13.35; 95% CI -6.71 to -0.54; P=.02). No adverse events were reported during the 3-year follow-up period.

CONCLUSIONS

The mHealth intervention, Run4Love, significantly reduced depressive symptoms among people living with HIV, and the intervention effects were sustained at 1-year and 3-year follow-ups. Further research is needed to explore the mechanisms of the long-term effects of mHealth interventions such as Run4Love and to implement these effective interventions among people living with HIV.

TRIAL REGISTRATION

Chinese Clinical Trial Registry ChiCTR-IPR-17012606; https://trialsearch.who.int/Trial2.aspx?TrialID=ChiCTR-IPR-17012606.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR2-10.2196/10274.

摘要

背景

新的研究表明,移动健康(mHealth)干预措施在降低 HIV 感染者的抑郁症状方面是有效的。这些研究大多只包括短期随访,关于长期效果的数据有限。

目的

本研究旨在评估一项名为“Run4Love”的随机对照试验在 1 年和 3 年随访时对 HIV 感染者抑郁症状的长期影响。

方法

2017 年 9 月至 2018 年 1 月,在中国广州招募了 300 名患有抑郁症状的 HIV 感染者,并将其随机分为干预组和对照组。干预组接受了为期 3 个月的“Run4Love”计划,包括改编的基于证据的认知行为应激管理课程和通过微信(腾讯)促进锻炼。对照组接受常规护理和营养小册子。主要结局是使用流行病学研究中心抑郁量表(CES-D)衡量抑郁症状的减少。本研究使用的数据是在基线和 1 年及 3 年随访时收集的。使用广义估计方程来检验 1 年和 3 年随访时的组间差异。

结果

大约一半的参与者在 1 年(149/300,49.7%)和 3 年(177/300,59%)随访时完成了评估。在 1 年随访时,与对照组相比,干预组的抑郁症状显著减轻(CES-D:从 23.9 降至 18.1,干预组;从 24.3 降至 23.3,对照组;平均-4.79,SD 13.56;95%CI -7.78 至-1.81;P=.002)。在 3 年随访时,两组间 CES-D 仍存在统计学差异(从 23.9 降至 20.5,干预组;从 24.3 降至 24.4,对照组;平均-3.63,SD 13.35;95%CI -6.71 至-0.54;P=.02)。在 3 年随访期间,没有报告不良事件。

结论

mHealth 干预措施“Run4Love”显著降低了 HIV 感染者的抑郁症状,干预效果在 1 年和 3 年随访时持续存在。需要进一步研究来探索 mHealth 干预措施(如“Run4Love”)的长期效果机制,并在 HIV 感染者中实施这些有效的干预措施。

试验注册

中国临床试验注册中心 ChiCTR-IPR-17012606;https://trialsearch.who.int/Trial2.aspx?TrialID=ChiCTR-IPR-17012606。

国际注册报告标识符(IRRID):RR2-10.2196/10274。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3470/9277532/2e0bcce7cf57/jmir_v24i6e36809_fig1.jpg

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