Randomized Controlled Pilot Trial of a Low-Touch Remotely-Delivered Values Intervention to Promote Adherence to Adjuvant Endocrine Therapy Among Breast Cancer Survivors

Author:

Arch Joanna J12ORCID,Crespi Catherine M3ORCID,Levin Michael E4,Genung Sarah R1,Nealis Madeline1,Mitchell Jill L5,Bright Emma E1,Albright Karen6,Magidson Jessica F7,Stanton Annette L891011

Affiliation:

1. Department of Psychology and Neuroscience, University of Colorado Boulder , 345 UCB Muenzinger, Boulder, CO, 80309-0345 , USA

2. Division of Cancer Prevention and Control, University of Colorado Cancer Center , Aurora, CO , USA

3. Fielding School of Public Health, Department of Biostatistics, University of California Los Angeles , Los Angeles, CA , USA

4. Department of Psychology, Utah State University , Logan, UT , USA

5. Rocky Mountain Cancer Centers-Boulder , Boulder, CO , USA

6. Department of Medicine, Division of General Internal Medicine, University of Colorado School of Medicine , Aurora, CO , USA

7. Department of Psychology, University of Maryland , College Park, MD , USA

8. Department of Psychology, University of California Los Angeles , Los Angeles, CA , USA

9. Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles , Los Angeles, CA , USA

10. Jonsson Comprehensive Cancer Center, University of California Los Angeles , Los Angeles, CA , USA

11. Semel Institute for Neuroscience, Cousins Center for Psychoneuroimmunology, University of California Los Angeles , Los Angeles, CA , USA

Abstract

Abstract Background Oral anti-cancer treatments such as adjuvant endocrine therapies (AET) for breast cancer survivors are commonly used but adherence is a challenge. Few low-touch, scalable interventions exist to increase ET adherence. Purpose To evaluate the acceptability, feasibility, and initial efficacy of a low-touch, remotely-delivered values plus AET education intervention (REACH) to promote AET adherence. Methods A mixed-methods trial randomized 88 breast cancer survivors 1:1 to REACH or Education alone. Wisepill real-time electronic adherence monitoring tracked monthly AET adherence during a 1-month baseline through 6-month follow-up (FU) (primary outcome). Patient-reported outcomes were evaluated through 3- and 6-month FU (secondary). Multiple indices of intervention feasibility and acceptability were evaluated. Qualitative exit interviews (n = 38) further assessed participants’ perceptions of feasibility/acceptability and recommendations for intervention adaptation. Results The trial showed strong feasibility and acceptability, with an eligible-to-enrolled rate of 85%, 100% completion of the main intervention sessions, and “good” intervention satisfaction ratings on average. For Wisepill-assessed AET adherence, REACH outperformed Education for Month 1 of FU (p = .027) and not thereafter. Participants in REACH maintained high adherence until Month 4 of FU, whereas in Education, adherence declined significantly in Month 1. Conditions did not differ in self-reported adherence, positive affective attitudes, future intentions, or necessity beliefs. REACH trended toward less negative AET attitudes than Education at 3-month FU (p = .057) reflecting improvement in REACH (p = .004) but not Education (p = .809). Exploratory moderator analyses showed that average to highly positive baseline AET affective attitudes and oncologist-patient communication each predicted higher adherence following REACH than Education; low levels did not. Participants identified recommendations to strengthen the interventions. Conclusions REACH, a low-touch values intervention, showed good feasibility and acceptability, and initial promise in improving objectively-assessed AET adherence among breast cancer survivors (relative to education alone). Future research should target improving REACH’s tailoring and endurance.

Funder

National Institutes of Health

National Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health,General Psychology

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