Patient perspectives on participation in the ENABLE II randomized controlled trial of a concurrent oncology palliative care intervention: Benefits and burdens

Author:

Maloney Cristine1,Lyons Kathleen Doyle2,Li Zhongze3,Hegel Mark2,Ahles Tim A4,Bakitas Marie5

Affiliation:

1. Department of Anesthesiology, Section of Palliative Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH; Department of Internal Medicine, Gifford Medical Center, Randolph, VT, USA

2. Department of Psychiatry, Dartmouth Medical School, Hanover, NH, USA

3. Biostatistics Shared Resource, Norris Cotton Cancer Center, Dartmouth College, Hanover, NH, USA

4. Department of Psychiatry, Memorial Sloan-Kettering Cancer Center, NY, USA

5. Department of Anesthesiology, Section of Palliative Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH; The Dartmouth Institute for Health Policy and Clinical Practice, Dartmouth Medical School, Hanover, NH, USA

Abstract

Background: ENABLE (Educate, Nurture, Advise Before Life Ends) II was one of the first randomized controlled trials (RCTs) examining the effects of a concurrent oncology palliative care intervention on quality of life, mood, and symptom control for advanced cancer patients and their caregivers. However, little is known about how participants experience early palliative care and the benefits and burdens of participating in a palliative care clinical trial. Aim: To gain a deeper understanding of participants’ perspectives of the intervention and palliative care trial participation. Design: A qualitative descriptive study using thematic analysis to determine benefits and burdens of a new palliative care intervention and trial participation. Setting/participants: Of the 72 participants who were alive when the study commenced, 53 agreed to complete an in-depth, semi-structured interview regarding the ENABLE II intervention and clinical trial participation. Results: Participants’ perceptions of intervention benefits were represented by four themes: enhanced problem-solving skills, better coping, feeling empowered, and feeling supported or reassured. Three themes related to trial participation: helping future patients and contributing to science, gaining insight through completion of questionnaires, and trial/intervention aspects to improve. Conclusions: The benefits of the intervention and the positive aspects of trial participation outweighed trial “burdens”. This study raises additional important questions relevant to future trial design and intervention development: when should a palliative care intervention be initiated and what aspects of self-care and healthy living should be offered in addition to palliative content for advanced cancer patients when they are feeling well?

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

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