Identifying the ‘Active Ingredients' of an Effective Psychological Intervention to Reduce Fear of Cancer Recurrence: A Process Evaluation
Purpose: Psychological interventions targeting fear of cancer recurrence (FCR) are effective in reducing fear and distress. Process evaluations are an important, yet scarce adjunct to published intervention trials, despite their utility in guiding the interpretation of study outcomes and optimizing...
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Published in | Frontiers in psychology Vol. 12; p. 661190 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
07.06.2021
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Abstract | Purpose:
Psychological interventions targeting fear of cancer recurrence (FCR) are effective in reducing fear and distress. Process evaluations are an important, yet scarce adjunct to published intervention trials, despite their utility in guiding the interpretation of study outcomes and optimizing intervention design for broader implementation. Accordingly, this paper reports the findings of a process evaluation conducted alongside a randomized controlled trial of a psychological intervention for melanoma patients.
Methods:
Men and women with a history of Stage 0–II melanoma at high-risk of developing new primary disease were recruited
via
High Risk Melanoma Clinics across Sydney, Australia and randomly allocated to receive the psychological intervention (
n
= 80) or usual care (
n
= 84). Intervention participants received a tailored psycho-educational resource and three individual psychotherapeutic sessions delivered
via
telehealth. Qualitative and quantitative data on intervention context, processes, and delivery (reach, dose, and fidelity), and mechanisms of impact (participant responses, moderators of outcome) were collected from a range of sources, including participant surveys, psychotherapeutic session audio-recordings, and clinical records.
Results:
Almost all participants reported using the psycho-educational resource (97%), received all intended psychotherapy sessions (96%), and reported high satisfaction with both intervention components. Over 80% of participants would recommend the intervention to others, and a small proportion (4%) found discussion of melanoma-related experiences confronting. Perceived benefits included enhanced doctor-patient communication, talking more openly with family members about melanoma, and improved coping. Of potential moderators, only higher FCR severity at baseline (pre-intervention) was associated with greater reductions in FCR severity (primary outcome) at 6-month follow-up (primary endpoint).
Conclusions:
Findings support the acceptability and feasibility of a psychological intervention to reduce FCR amongst individuals at high risk of developing another melanoma. Implementation into routine melanoma care is an imperative next step, with FCR screening recommended to identify those most likely to derive the greatest psychological benefit. |
---|---|
AbstractList | Purpose:
Psychological interventions targeting fear of cancer recurrence (FCR) are effective in reducing fear and distress. Process evaluations are an important, yet scarce adjunct to published intervention trials, despite their utility in guiding the interpretation of study outcomes and optimizing intervention design for broader implementation. Accordingly, this paper reports the findings of a process evaluation conducted alongside a randomized controlled trial of a psychological intervention for melanoma patients.
Methods:
Men and women with a history of Stage 0–II melanoma at high-risk of developing new primary disease were recruited
via
High Risk Melanoma Clinics across Sydney, Australia and randomly allocated to receive the psychological intervention (
n
= 80) or usual care (
n
= 84). Intervention participants received a tailored psycho-educational resource and three individual psychotherapeutic sessions delivered
via
telehealth. Qualitative and quantitative data on intervention context, processes, and delivery (reach, dose, and fidelity), and mechanisms of impact (participant responses, moderators of outcome) were collected from a range of sources, including participant surveys, psychotherapeutic session audio-recordings, and clinical records.
Results:
Almost all participants reported using the psycho-educational resource (97%), received all intended psychotherapy sessions (96%), and reported high satisfaction with both intervention components. Over 80% of participants would recommend the intervention to others, and a small proportion (4%) found discussion of melanoma-related experiences confronting. Perceived benefits included enhanced doctor-patient communication, talking more openly with family members about melanoma, and improved coping. Of potential moderators, only higher FCR severity at baseline (pre-intervention) was associated with greater reductions in FCR severity (primary outcome) at 6-month follow-up (primary endpoint).
Conclusions:
Findings support the acceptability and feasibility of a psychological intervention to reduce FCR amongst individuals at high risk of developing another melanoma. Implementation into routine melanoma care is an imperative next step, with FCR screening recommended to identify those most likely to derive the greatest psychological benefit. Purpose: Psychological interventions targeting fear of cancer recurrence (FCR) are effective in reducing fear and distress. Process evaluations are an important, yet scarce adjunct to published intervention trials, despite their utility in guiding the interpretation of study outcomes and optimizing intervention design for broader implementation. Accordingly, this paper reports the findings of a process evaluation conducted alongside a randomized controlled trial of a psychological intervention for melanoma patients.Methods: Men and women with a history of Stage 0–II melanoma at high-risk of developing new primary disease were recruited via High Risk Melanoma Clinics across Sydney, Australia and randomly allocated to receive the psychological intervention (n = 80) or usual care (n = 84). Intervention participants received a tailored psycho-educational resource and three individual psychotherapeutic sessions delivered via telehealth. Qualitative and quantitative data on intervention context, processes, and delivery (reach, dose, and fidelity), and mechanisms of impact (participant responses, moderators of outcome) were collected from a range of sources, including participant surveys, psychotherapeutic session audio-recordings, and clinical records.Results: Almost all participants reported using the psycho-educational resource (97%), received all intended psychotherapy sessions (96%), and reported high satisfaction with both intervention components. Over 80% of participants would recommend the intervention to others, and a small proportion (4%) found discussion of melanoma-related experiences confronting. Perceived benefits included enhanced doctor-patient communication, talking more openly with family members about melanoma, and improved coping. Of potential moderators, only higher FCR severity at baseline (pre-intervention) was associated with greater reductions in FCR severity (primary outcome) at 6-month follow-up (primary endpoint).Conclusions: Findings support the acceptability and feasibility of a psychological intervention to reduce FCR amongst individuals at high risk of developing another melanoma. Implementation into routine melanoma care is an imperative next step, with FCR screening recommended to identify those most likely to derive the greatest psychological benefit. |
Author | Tesson, Stephanie Cust, Anne E. Morton, Rachael L. Costa, Daniel S. J. Kan, Janice M. Dieng, Mbathio Butow, Phyllis N. Menzies, Scott W. Kasparian, Nadine A. Mann, Graham J. Mireskandari, Shab |
AuthorAffiliation | 6 The Sydney Melanoma Diagnostic Centre, Royal Prince Alfred Hospital , Sydney, NSW , Australia 8 School of Psychology, University of Sydney , Sydney, NSW , Australia 12 Cincinnati Children's Center for Heart Disease and Mental Health, Heart Institute and the Division of Behavioral Medicine & Clinical Psychology, Cincinnati Children's Hospital , Cincinnati, OH , United States 1 Discipline of Paediatrics, School of Women's and Children's Health, UNSW Medicine, The University of New South Wales , Sydney, NSW , Australia 9 Melanoma Institute Australia, The University of Sydney , Sydney, NSW , Australia 2 NHMRC Clinical Trials Centre, The University of Sydney , Sydney, NSW , Australia 3 Centre for Medical Psychology and Evidence-Based Decision-Making, School of Psychology, The University of Sydney , Sydney, NSW , Australia 10 John Curtin School of Medical Research, College of Health and Medicine, The Australian National University , Canberra, ACT , Australia 4 Psycho-Oncology Co-operative Research |
AuthorAffiliation_xml | – name: 4 Psycho-Oncology Co-operative Research Group, School of Psychology, The University of Sydney , Sydney, NSW , Australia – name: 9 Melanoma Institute Australia, The University of Sydney , Sydney, NSW , Australia – name: 2 NHMRC Clinical Trials Centre, The University of Sydney , Sydney, NSW , Australia – name: 8 School of Psychology, University of Sydney , Sydney, NSW , Australia – name: 13 Department of Pediatrics, University of Cincinnati College of Medicine , Cincinnati, OH , United States – name: 11 Cancer Epidemiology and Prevention Research, Sydney School of Public Health, The University of Sydney , Sydney, NSW , Australia – name: 5 Discipline of Dermatology, Sydney Medical School, The University of Sydney , Sydney, NSW , Australia – name: 7 Pain Management Research Institute, The University of Sydney at Royal North Shore Hospital , Sydney, NSW , Australia – name: 1 Discipline of Paediatrics, School of Women's and Children's Health, UNSW Medicine, The University of New South Wales , Sydney, NSW , Australia – name: 12 Cincinnati Children's Center for Heart Disease and Mental Health, Heart Institute and the Division of Behavioral Medicine & Clinical Psychology, Cincinnati Children's Hospital , Cincinnati, OH , United States – name: 6 The Sydney Melanoma Diagnostic Centre, Royal Prince Alfred Hospital , Sydney, NSW , Australia – name: 10 John Curtin School of Medical Research, College of Health and Medicine, The Australian National University , Canberra, ACT , Australia – name: 3 Centre for Medical Psychology and Evidence-Based Decision-Making, School of Psychology, The University of Sydney , Sydney, NSW , Australia |
Author_xml | – sequence: 1 givenname: Janice M. surname: Kan fullname: Kan, Janice M. – sequence: 2 givenname: Mbathio surname: Dieng fullname: Dieng, Mbathio – sequence: 3 givenname: Phyllis N. surname: Butow fullname: Butow, Phyllis N. – sequence: 4 givenname: Shab surname: Mireskandari fullname: Mireskandari, Shab – sequence: 5 givenname: Stephanie surname: Tesson fullname: Tesson, Stephanie – sequence: 6 givenname: Scott W. surname: Menzies fullname: Menzies, Scott W. – sequence: 7 givenname: Daniel S. J. surname: Costa fullname: Costa, Daniel S. J. – sequence: 8 givenname: Rachael L. surname: Morton fullname: Morton, Rachael L. – sequence: 9 givenname: Graham J. surname: Mann fullname: Mann, Graham J. – sequence: 10 givenname: Anne E. surname: Cust fullname: Cust, Anne E. – sequence: 11 givenname: Nadine A. surname: Kasparian fullname: Kasparian, Nadine A. |
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Cites_doi | 10.1007/s00520-012-1685-3 10.1093/pubmed/fdi031 10.1016/j.ejso.2012.12.017 10.1001/jamadermatol.2014.514 10.1002/pon.4516 10.1200/JCO.2016.68.2278 10.1177/109019810002700202 10.1371/journal.pone.0234124 10.1002/pon.4103 10.1007/s00520-016-3339-3 10.1186/s40359-015-0074-3 10.1136/jech-2013-202869 10.1002/pon.3022 10.1136/bmjopen-2016-012153 10.1002/cncr.31539 10.1007/s00520-020-05464-3 10.1037/a0018378 10.1136/bmjopen-2016-015195 10.1080/09544820903317001 10.2147/PRBM.S231577 10.1007/s40258-019-00483-6 10.1002/pon.3165 10.1002/pon.3243 10.1007/s00520-016-3248-5 10.1001/archpsyc.58.5.494 10.1007/s00520-014-2414-x 10.1007/s11764-015-0434-2 10.1200/JCO.2017.73.1257 10.1007/s11764-013-0272-z 10.1159/000228247 10.1002/pon.3718 10.1111/bjd.17990 10.1016/S0936-6555(05)80321-8 10.1177/1049732312448542 10.1002/pon.3114 10.1007/s00520-008-0444-y 10.1136/bmj.h1258 10.1016/j.soncn.2013.06.007 10.1002/pon.4018 10.1002/pon.5350 |
ContentType | Journal Article |
Copyright | Copyright © 2021 Kan, Dieng, Butow, Mireskandari, Tesson, Menzies, Costa, Morton, Mann, Cust and Kasparian. 2021 Kan, Dieng, Butow, Mireskandari, Tesson, Menzies, Costa, Morton, Mann, Cust and Kasparian |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Andreas Dinkel, Technical University of Munich, Germany This article was submitted to Psycho-Oncology, a section of the journal Frontiers in Psychology Reviewed by: Colsom Bashir, Christie Hospital NHS Foundation Trust, United Kingdom; Karen Holtmaat, Vrije Universiteit Amsterdam, Netherlands |
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References | Crist (B11) 2013; 22 Mutsaers (B34) 2016; 24 Dieng (B16) 2019; 17 Bowling (B5) 2005; 27 McLoone (B29); 22 Moore (B32) 2015; 350 Dieng (B17) 2020; 182 Dieng (B13); 6 Butow (B7) 2018; 32 Lebel (B24) 2017; 26 Dieng (B12); 34 Maloney (B27) 2014; 150 Kasparian (B20) 2013; 29 Rudy (B36) 2020; 29 Simard (B39) 2009; 17 Abbass (B1) 2009; 78 Dieng (B14) 2017; 7 Baranowski (B2) 2000; 27 Baughan (B3) 1993; 5 Classen (B9) 2001; 58 Fu (B19) 2020; 28 Sarkar (B37) 2015; 9 Dieng (B15) 2015; 3 McLoone (B28); 22 Moore (B31) 2014; 68 Butow (B8) 2017; 35 Kasparian (B21) 2016; 24 Stamataki (B42) 2015; 23 Beesley (B4) 2015; 24 McLoone (B30) 2012; 22 Breitbart (B6) 2018; 124 Costa (B10) 2016; 25 Lim (B26) 2010; 21 Morton (B33) 2013; 39 Lebel (B23) 2020; 15 Shedler (B38) 2010; 65 Lebel (B25) 2013; 21 Koch (B22) 2013; 22 Smith (B41) 2020; 13 Simard (B40) 2013; 7 Fardell (B18) 2018; 27 Mutsaers (B35) 2020; 66 |
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Psychological interventions targeting fear of cancer recurrence (FCR) are effective in reducing fear and distress. Process evaluations are an... Purpose: Psychological interventions targeting fear of cancer recurrence (FCR) are effective in reducing fear and distress. Process evaluations are an... |
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StartPage | 661190 |
SubjectTerms | fear cancer recurrence intervention melanoma process evaluation psychological stress Psychology survivorship |
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Title | Identifying the ‘Active Ingredients' of an Effective Psychological Intervention to Reduce Fear of Cancer Recurrence: A Process Evaluation |
URI | https://search.proquest.com/docview/2544880982 https://pubmed.ncbi.nlm.nih.gov/PMC8215538 https://doaj.org/article/484c64458a0a42db88ec09681980a043 |
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