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.
中科院分区:
文献类型:
--
作者:
Smith, Isabelle S.;Wallace, Rebecca;Wellecke, Cornelia;Bind, Marie-Abele;Weihs, Karen L.;Bei, Bei;Wiley, Joshua F.
关键词:
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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影响因子:
2.6
作者:
Gallagher, Matthew W.;Sauer-Zavala, Shannon E.;Barlow, David H.
通讯作者:
Barlow, David H.
DOI:
10.1093/jnci/djy177
发表时间:
2018-12-01
期刊:
Journal of the National Cancer Institute
影响因子:
--
作者:
Carreira H;Williams R;Müller M;Harewood R;Stanway S;Bhaskaran K
通讯作者:
Bhaskaran K
影响因子:
3.8
作者:
Hallion, Lauren S.;Steinman, Shari A.;Diefenbach, Gretchen J.
通讯作者:
Diefenbach, Gretchen J.
DOI:
10.1016/j.jbtep.2019.101487
发表时间:
2019-12-01
影响因子:
1.8
作者:
Harris, Kelly R.;Norton, Peter J.
通讯作者:
Norton, Peter J.
DOI:
10.1016/s0005-7916(00)00012-4
发表时间:
2000-06-01
影响因子:
1.8
作者:
Devilly, GJ;Borkovec, TD
通讯作者:
Borkovec, TD