Assessing an Internet-Delivered, Emotion-Focused Intervention Compared With a Healthy Lifestyle Active Control Intervention in Improving Mental Health in Cancer Survivors: Protocol for a Randomized Controlled Trial.

Assessing an Internet-Delivered, Emotion-Focused Intervention Compared With a Healthy Lifestyle Active Control Intervention in Improving Mental Health in Cancer Survivors: Protocol for a Randomized Controlled Trial.
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与健康的生活方式控制干预措施相比,评估互联网传递的,以情感为中心的干预措施来改善癌症幸存者的心理健康:随机对照试验的协议。

DOI:
10.2196/36658
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发表时间:
2022-07-27
影响因子:
1.7
通讯作者:
Wiley, Joshua F.
Wiley, Joshua F.
中科院分区:
其他
文献类型:
--
作者:
Smith, Isabelle S.;Wallace, Rebecca;Wellecke, Cornelia;Bind, Marie-Abele;Weihs, Karen L.;Bei, Bei;Wiley, Joshua F.

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癌症幸存者容易经历焦虑和抑郁的症状,并可能受益于专注于改善情绪调节的可获得的干预措施。CanCope Mind(CM)是一种互联网传递的干预措施,改编自情绪障碍跨诊断治疗统一协议,以改善情绪调节并支持癌症幸存者的心理健康。该协议旨在提供CanCope研究的概要,该研究是一项试验,比较了为癌症幸存者设计的适用于统一协议的互联网传递干预(CM)与积极控制条件--互联网传递的健康生活方式干预-CanCope Lifestyle(CL)的疗效。主要目的是评估和比较这两种干预措施在改善情绪调节、焦虑和抑郁症状以及生活质量方面的效果。次要目标包括评估CM干预的机制。这项试验是一项双臂随机对照试验,将癌症幸存者分配到CM或CL。这两种干预措施都包括4个基于网络的模块,预计参与者至少需要8周时间才能完成。参与者的心理和身体健康将通过在基线(T0)、每个模块之间(T1、T2和T3)、干预后立即(T4)和3个月随访(T5)时的自我报告调查来评估。这项研究的目标是招募110名完成T4课程的参与者。CanCope研究于2020年9月开始招募。共有224名参与者被随机分为CM组(n=110,49.1%)和CL组(n=114,50.9%)。这是开发和调查针对癌症幸存者的网络干预效果的首批试验之一,该干预专门针对情绪调节。澳大利亚临床试验法案12620000943943;https://tinyurl.com/b3z9cjsp DERR112620000943943-10.2196/12439
Cancer survivors are vulnerable to experiencing symptoms of anxiety and depression and may benefit from accessible interventions focused on improving emotion regulation. CanCope Mind (CM) was developed as an internet-delivered intervention adapted from the Unified Protocol for Transdiagnostic Treatment of Emotional Disorders to improve emotion regulation and support the mental health of cancer survivors. This protocol aims to provide an outline of the CanCope Study, a trial comparing the efficacy of a Unified Protocol–adapted internet-delivered intervention (CM) designed for cancer survivors compared with an active control condition—an internet-delivered healthy lifestyle intervention, CanCope Lifestyle (CL). The primary aim is to assess and compare the efficacy of both interventions in improving emotion regulation, anxiety and depressive symptoms, and quality of life. The secondary aims involve assessing the mechanisms of the CM intervention. This trial is a 2-arm randomized controlled trial that allocates cancer survivors to either CM or CL. Both interventions comprise 4 web-based modules and are expected to take participants at least 8 weeks to complete. Participants’ mental and physical health will be assessed via self-reported surveys at baseline (T0), between each module (T1, T2, and T3), immediately after the intervention (T4), and at 3-month follow-up (T5). The study aims to recruit 110 participants who have completed T4. The CanCope study began recruitment in September 2020. A total of 224 participants have been randomized to the CM (n=110, 49.1%) and CL (n=114, 50.9%) groups. This is one of the first trials to develop and investigate the efficacy of a web-based intervention for cancer survivors that specifically targets emotion regulation. Australian Clinical Trials ACTRN12620000943943; https://tinyurl.com/b3z9cjsp DERR1-10.2196/36658
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