ConquerFear-Group: A randomized controlled trial of an online-delivered group-based psychological intervention for fear of cancer recurrence in breast cancer survivors
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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. / Tauber, Nina M.; O’Toole, Mia S.; Jensen, Anders B.; Butow, Phyllis N.; Thewes, Belinda; Elkjær, Emma; Knutzen, Sofie; von Heymann, Annika; Johansen, Christoffer; Zachariae, Robert.
I: Psycho-Oncology, Bind 32, Nr. 9, 2023, s. 1424-1432.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - ConquerFear-Group
T2 - A randomized controlled trial of an online-delivered group-based psychological intervention for fear of cancer recurrence in breast cancer survivors
AU - Tauber, Nina M.
AU - O’Toole, Mia S.
AU - Jensen, Anders B.
AU - Butow, Phyllis N.
AU - Thewes, Belinda
AU - Elkjær, Emma
AU - Knutzen, Sofie
AU - von Heymann, Annika
AU - Johansen, Christoffer
AU - Zachariae, Robert
N1 - Publisher Copyright: © 2023 The Authors. Psycho-Oncology published by John Wiley & Sons Ltd.
PY - 2023
Y1 - 2023
N2 - Objective: 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). Methods: 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. Results: 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. Conclusions: 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.
AB - Objective: 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). Methods: 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. Results: 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. Conclusions: 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.
KW - anxiety
KW - cancer
KW - cancer survivorship
KW - fear
KW - psychooncology
KW - psychosocial intervention
U2 - 10.1002/pon.6193
DO - 10.1002/pon.6193
M3 - Journal article
C2 - 37489745
AN - SCOPUS:85165553953
VL - 32
SP - 1424
EP - 1432
JO - Psycho-Oncology
JF - Psycho-Oncology
SN - 1057-9249
IS - 9
ER -
ID: 396723954