A pilot randomized controlled trial (RCT) of daily versus weekly interactive voice response calls to support adherence among antiretroviral treatment patients in India.

IF 2.2 Q2 HEALTH CARE SCIENCES & SERVICES mHealth Pub Date : 2020-10-05 eCollection Date: 2020-01-01 DOI:10.21037/mhealth-19-248a
Dallas Swendeman, Anne E Fehrenbacher, Soma Roy, Protim Ray, Stephanie Sumstine, Aaron Scheffler, Rishi Das, Smaraijt Jana
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Abstract

Background: There are more than two million people living with HIV (PLH) in India, with more than 30% on antiretroviral treatment (ART) estimated to be non-adherent. This study aimed to (I) document adherence rates and related factors among ART patients in a large ART clinic in India, and (II) pilot test daily and weekly interactive voice response (IVR) calls to improve ART adherence and related outcomes.

Methods: ART patients reporting missing at least one dose in prior 6 months (N=362) were enrolled and assessed via self-report and medical record review. Participants were randomized to one of two conditions: (I) twice-daily IVR call reminders with self-management support messaging, plus a weekly IVR adherence assessment; or (II) an attention control, with only weekly IVR adherence assessment. Participants completed study assessments at baseline, 2-, 4-, and 6-months with high retention (88% to 96%).

Results: Intention-to-treat analyses found limited support for intervention effects for improving or maintaining ART adherence or CD4 counts between the two study arms over 6-months follow-up. Adherence increased significantly in the six months prior to baseline from about 65% to >95% with perfect adherence based on pill counts from medical records and consistent with patient self-report measures, which presented ceiling effects for detecting improvements in ART adherence in response to IVR intervention exposure. There was also limited support for intervention effects on secondary, self-management outcomes.

Conclusions: High levels of adherence were sustained throughout the 6-month RCT. IVR regulation changes in India delayed study launch for 6 months, which likely allowed mobilization of improved adherence at the clinic, provider and patient levels in anticipation of the study launch. Therefore, ceiling effects limited inferences on intervention effects to improve adherence. Results suggest that clinic-level adherence monitoring may be sufficient to mobilize adherence improvements by providers and patients.

Trial registration: ClinicalTrials.gov registration #NCT02118454.

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为支持印度抗逆转录病毒治疗患者坚持治疗,进行了一项试点随机对照试验 (RCT),对每天与每周交互式语音应答电话进行对比。
背景:印度有 200 多万艾滋病病毒感染者(PLH),据估计 30% 以上的抗逆转录病毒疗法(ART)患者没有坚持治疗。本研究旨在(I)记录印度一家大型抗逆转录病毒疗法诊所中抗逆转录病毒疗法患者的依从率及相关因素;(II)对每日和每周的交互式语音应答(IVR)电话进行试点测试,以改善抗逆转录病毒疗法的依从性及相关结果:方法: 登记并通过自我报告和病历审查对报告在过去 6 个月中至少漏服一次药物的抗逆转录病毒疗法患者(362 人)进行评估。参与者被随机分配到两种条件之一:(I) 每天两次IVR呼叫提醒,提供自我管理支持信息,加上每周IVR依从性评估;或(II) 注意力对照,仅每周进行IVR依从性评估。参与者在基线、2个月、4个月和6个月时完成了研究评估,保留率较高(88%至96%):结果:意向治疗分析发现,在为期 6 个月的随访中,两个研究臂对改善或维持抗逆转录病毒疗法依从性或 CD4 细胞计数的干预效果支持有限。基线前 6 个月的依从性明显提高,从约 65% 提高到大于 95%,依从性完全符合医疗记录中的药片计数,并与患者自我报告的测量结果一致,这为检测 IVR 干预暴露对 ART 依从性的改善带来了上限效应。此外,干预对次级自我管理结果的影响也有限:结论:在为期 6 个月的 RCT 中,高水平的依从性得以维持。印度 IVR 管理条例的改变将研究的启动时间推迟了 6 个月,这很可能使诊所、医疗服务提供者和患者的依从性在研究启动前得到了改善。因此,天花板效应限制了对改善依从性的干预效果的推断。结果表明,诊所层面的依从性监测可能足以调动医疗服务提供者和患者改善依从性的积极性:试验注册:ClinicalTrials.gov 注册 #NCT02118454。
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