Feasibility and Preliminary Effectiveness of Behavioral Activation for Patients with Cancer and Depression in Japan.

IF 1.1 Q4 HEALTH CARE SCIENCES & SERVICES Palliative medicine reports Pub Date : 2023-01-01 DOI:10.1089/pmr.2023.0020
Takatoshi Hirayama, Yuko Ogawa, Yuko Yanai, Akie Shindo, Moeko Tanaka, Shin-Ichi Suzuki
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Abstract

Background: Though the effectiveness of behavioral activation (BA) for patients with cancer and depression were reported, there is no evidence in Japan.

Objectives: This study aimed at examining the feasibility and preliminary effectiveness of BA for patients with cancer and depression in Japan.

Methods: This pre-post study without a control group was conducted in patients with cancer and depression in Japan. The program completion rate was compared with those of previous studies to examine feasibility. To examine the preliminary effectiveness, outcomes were evaluated four times: before and immediately after the program, and two weeks and three months after the program ended. The primary outcome was the remission rate of depression using the 17-item version of the GRID Hamilton Rating Scale for Depression (HAMD17). Secondary outcomes were self-reported depression, anxiety, quality of life, changes in behavior, values, and perceived reward of activity and environmental factors. Pre- and post-program data were compared using paired-samples t-tests, and data obtained at four time points were analyzed using one-way repeated-measures analysis of variance.

Results: Of the 68 patients recruited from February 2018 to January 2022, 32 were registered. The completion rate was 75% (24/32), which was similar to previous studies. The total HAMD17 score significantly improved after the program. The remission rate of depression was 62.5% (20/32), which was above the defined threshold value (30%). All but two secondary outcomes significantly improved after the program (p < 0.05).

Conclusions: The feasibility and preliminary effectiveness of BA for patients with cancer and depression in Japan were suggested.

The Clinical Trial Registration number: UMIN 000036104.

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日本癌症和抑郁症患者行为激活的可行性和初步效果。
背景:虽然行为激活(BA)对癌症和抑郁症患者的有效性有报道,但在日本尚无证据。目的:本研究旨在探讨BA治疗日本癌症和抑郁症患者的可行性和初步效果。方法:在日本的癌症和抑郁症患者中进行无对照组的前-后研究。将项目完成率与以往研究的完成率进行比较,以检验项目的可行性。为了检查初步的有效性,结果评估了四次:在计划之前和之后,以及计划结束后的两周和三个月。主要结果是使用GRID汉密尔顿抑郁量表(HAMD17)的17项版本的抑郁缓解率。次要结果是自我报告的抑郁、焦虑、生活质量、行为改变、价值观、活动和环境因素的感知奖励。使用配对样本t检验比较计划前后的数据,并使用单向重复测量方差分析分析四个时间点的数据。结果:在2018年2月至2022年1月招募的68名患者中,32名患者注册。完成率为75%(24/32),与以往研究相似。HAMD17总分在项目结束后显著提高。抑郁症的缓解率为62.5%(20/32),高于定义的阈值(30%)。除两项次要结局外,其余次要结局均有显著改善(p)。结论:建议BA在日本治疗癌症和抑郁症患者的可行性和初步有效性。临床试验注册号:UMIN 000036104。
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审稿时长
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