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ConquerFear‐Group: A randomized controlled trial of an online‐delivered group‐based psychological intervention for fear of cancer recurrence in breast cancer survivors

随机对照试验 担心 医学 乳腺癌 心理干预 物理疗法 注意 癌症 沉思 焦虑 临床心理学 内科学 精神科 认知
作者
Nina M. Tauber,Mia Skytte O’Toole,Anders Bonde Jensen,Phyllis Butow,Belinda Thewes,Emma Elkjær,Sofie Møgelberg Knutzen,Annika von Heymann,Christoffer Johansen,Robert Zachariae
出处
期刊:Psycho-oncology [Wiley]
卷期号:32 (9): 1424-1432
标识
DOI:10.1002/pon.6193
摘要

Fear of cancer recurrence (FCR) is a distressing concern among cancer survivors. Interventions to address FCR need to be effective but also accessible and low cost. This randomized controlled trial evaluated the efficacy of an online group-based psychological intervention for FCR (ConquerFear-Group).Eligible breast cancer (BC) survivors had completed primary treatment 3 months-5 years previously, were ≥18 years, and scored ≥22 on the Fear of Cancer Recurrence Inventory-Short Form (FCRI-SF). Participants were randomized to online ConquerFear-Group (focusing on metacognitive strategies, values-clarification, and education about follow-up behavior) or online group-based relaxation training (active control). Questionnaires were completed at baseline (T1), 1 week post-intervention (T2), three (T3) and six (T4) months later. The primary outcome was FCR (FCRI total). A number of secondary and process outcomes were also collected. Treatment effects were evaluated with mixed linear models.Of 866 eligible BC survivors, 475 (55%) completed the FCR screening, and 85 (18%) were randomized to ConquerFear-Group or relaxation training (2 × 6 groups). Compared with control participants, ConquerFear-Group participants experienced larger reductions in FCR (Cohen's d = 0.47, p = 0.001) and FCR severity (d = 0.57, p < 0.001), as well as mindfulness and decentering from baseline through follow-up, and improvements in emotion regulation (T2), worry (T2, T3) and rumination (T2) at some time points.The results demonstrated statistically significant and stable effects of ConquerFear-Group on FCR that were maintained over a 6-month period. It is suggested to investigate the program in a real-life setting, where a pragmatic trial can further demonstrate feasibility and effectiveness.

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