TY - JOUR
T1 - Randomized trial of ConquerFear
T2 - A novel, theoretically based psychosocial intervention for fear of cancer recurrence
AU - Butow, Phyllis N.
AU - Turner, Jane
AU - Gilchrist, Jemma
AU - Sharpe, Louise
AU - Smith, Allan Ben
AU - Fardell, Joanna E.
AU - Tesson, Stephanie
AU - O'Connell, Rachel
AU - Girgis, Afaf
AU - Gebski, Val J.
AU - Asher, Rebecca
AU - Mihalopoulos, Cathrine
AU - Bell, Melanie L.
AU - Zola, Karina Grunewald
AU - Beith, Jane
AU - Thewes, Belinda
N1 - Publisher Copyright:
© 2017 by American Society of Clinical Oncology.
PY - 2017/12/20
Y1 - 2017/12/20
N2 - Purpose: Fear of cancer recurrence (FCR) is prevalent, distressing, and long lasting. This study evaluated the impact of a theoretically/empirically based intervention (ConquerFear) on FCR. Methods: Eligible survivors had curable breast or colorectal cancer or melanoma, had completed treatment (not including endocrine therapy) 2 months to 5 years previously, were age > 18 years, and had scores above the clinical cutoff on the FCR Inventory (FCRI) severity subscale at screening. Participants were randomly assigned at a one-to-one ratio to either five face-to-face sessions of ConquerFear (attention training, metacognitions, acceptance/mindfulness, screening behavior, and values-based goal setting) or an attention control (Taking-it-Easy relaxation therapy). Participants completed questionnaires at baseline (T0), immediately post-therapy (T1), and 3 (T2) and 6 months (T3) later. The primary outcome was FCRI total score. Results: Of 704 potentially eligible survivors from 17 sites and two online databases, 533 were contactable, of whom 222 (42%) consented; 121 were randomly assigned to intervention and 101 to control. Study arms were equivalent at baseline on all measured characteristics. ConquerFear participants had clinically and statistically greater improvements than control participants from T0 to T1 on FCRI total (P <.001) and severity subscale scores (P =.001), which were maintained at T2 (P =.017 and P =.023, respectively) and, for FCRI total only, at T3 (P =.018), and from T0 to T1 on three FCRI subscales (coping, psychological distress, and triggers) as well as in general anxiety, cancer-specific distress (total), and mental quality of life and metacognitions (total). Differences in FCRI psychological distress and cancer-specific distress (total) remained significantly different at T3. Conclusion: This randomized trial demonstrated efficacy of ConquerFear compared with attention control (Taking-it-Easy) in reduction of FCRI total scores immediately post-therapy and 3 and 6 months later and in many secondary outcomes immediately post-therapy. Cancer-specific distress (total) remained more improved at 3- and 6-month follow-up.
AB - Purpose: Fear of cancer recurrence (FCR) is prevalent, distressing, and long lasting. This study evaluated the impact of a theoretically/empirically based intervention (ConquerFear) on FCR. Methods: Eligible survivors had curable breast or colorectal cancer or melanoma, had completed treatment (not including endocrine therapy) 2 months to 5 years previously, were age > 18 years, and had scores above the clinical cutoff on the FCR Inventory (FCRI) severity subscale at screening. Participants were randomly assigned at a one-to-one ratio to either five face-to-face sessions of ConquerFear (attention training, metacognitions, acceptance/mindfulness, screening behavior, and values-based goal setting) or an attention control (Taking-it-Easy relaxation therapy). Participants completed questionnaires at baseline (T0), immediately post-therapy (T1), and 3 (T2) and 6 months (T3) later. The primary outcome was FCRI total score. Results: Of 704 potentially eligible survivors from 17 sites and two online databases, 533 were contactable, of whom 222 (42%) consented; 121 were randomly assigned to intervention and 101 to control. Study arms were equivalent at baseline on all measured characteristics. ConquerFear participants had clinically and statistically greater improvements than control participants from T0 to T1 on FCRI total (P <.001) and severity subscale scores (P =.001), which were maintained at T2 (P =.017 and P =.023, respectively) and, for FCRI total only, at T3 (P =.018), and from T0 to T1 on three FCRI subscales (coping, psychological distress, and triggers) as well as in general anxiety, cancer-specific distress (total), and mental quality of life and metacognitions (total). Differences in FCRI psychological distress and cancer-specific distress (total) remained significantly different at T3. Conclusion: This randomized trial demonstrated efficacy of ConquerFear compared with attention control (Taking-it-Easy) in reduction of FCRI total scores immediately post-therapy and 3 and 6 months later and in many secondary outcomes immediately post-therapy. Cancer-specific distress (total) remained more improved at 3- and 6-month follow-up.
UR - http://www.scopus.com/inward/record.url?scp=85038402962&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85038402962&partnerID=8YFLogxK
U2 - 10.1200/JCO.2017.73.1257
DO - 10.1200/JCO.2017.73.1257
M3 - Article
C2 - 29095681
AN - SCOPUS:85038402962
SN - 0732-183X
VL - 35
SP - 4066
EP - 4077
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 36
ER -