A telephone-based education and support intervention for Rural Breast Cancer Survivors: a randomized controlled trial comparing two implementation strategies in rural Florida.


Journal

Journal of cancer survivorship : research and practice
ISSN: 1932-2267
Titre abrégé: J Cancer Surviv
Pays: United States
ID NLM: 101307557

Informations de publication

Date de publication:
08 2020
Historique:
received: 25 08 2019
accepted: 12 02 2020
pubmed: 12 3 2020
medline: 16 12 2020
entrez: 12 3 2020
Statut: ppublish

Résumé

To compare two implementation telephone-based strategies of an evidence-based educational and support intervention to Rural Breast Cancer Survivors (RBCS) in which education was delivered early or after the support component. Florida RBCS participated in a 12-month randomized clinical trial (RCT) with two arms: Early Education and Support (EE-S) and Support and Delayed Education (S-DE). Arms differed in the timing of 6 support and 3 education sessions. Main outcome was quality of life (QOL, SF-36 physical and mental composite scores [PCS, MCS]). Secondary outcomes were depressive symptoms (Centers for Epidemiologic Studies Depression Scale, CES-D), mood (Profile of Mood States, POMS), and social support (Medical Outcomes Study Social Support Survey, MOS-SSS). Outcomes were analyzed longitudinally using repeated measures models fitted with linear mixed methods. Of 432 RBCS (mean 25.6 months from diagnosis), about 48% were 65+, 73% married/partnered, and 28% with ≤high school education. There were no differences between EE-S and S-DE in demographics or outcomes at baseline (mean (standard deviation): SF-36 PCS, 44.88 (10.6) vs. 45.08 (10.6); MCS, 49.45 (11.1) vs. 48.1 (11.9); CES-D, 10.11 (9.8) vs. 10.86 (10.5); POMS-SF, 23.95 (38.6) vs. 26.35 (38.8); MOS-SSS, 79.2 (21.2) vs. 78.66 (21.2)) or over time. One exception was slightly worse mean scores at month 9 in MCS (Cohen's d, - 0.22; 95% CI, - 0.38, - 0.06) and POMS (Cohen's d, 0.23; 95% CI, 0.07, 0.39) for EE-S vs. S-DE. The implementation strategies were equivalent. Enhancing support may be considered before delivering not-in-person interventions to RBCS.

Identifiants

pubmed: 32157608
doi: 10.1007/s11764-020-00866-y
pii: 10.1007/s11764-020-00866-y
pmc: PMC7365751
mid: NIHMS1574495
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

494-503

Subventions

Organisme : NCI NIH HHS
ID : R01 CA120638
Pays : United States

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Auteurs

Karen Meneses (K)

School of Nursing, Office of Research and Scholarship, University of Alabama at Birmingham, Birmingham, AL, USA.
O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.

Maria Pisu (M)

O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA. mpisu@uab.edu.
School of Medicine, Division of Preventive Medicine, University of Alabama at Birmingham, MT 636, 1720 2nd Avenue South, Birmingham, AL, 35294-4410, USA. mpisu@uab.edu.

Andres Azuero (A)

School of Nursing, Office of Research and Scholarship, University of Alabama at Birmingham, Birmingham, AL, USA.

Rachel Benz (R)

School of Nursing, Office of Research and Scholarship, University of Alabama at Birmingham, Birmingham, AL, USA.

Xiaogang Su (X)

Department of Mathematical Sciences, The University of Texas at El Paso, El Paso, TX, USA.

Patrick McNees (P)

School of Health Professions, University of Alabama at Birmingham, Birmingham, AL, USA.
PK LifeSciences Corp, Birmingham, AL, USA.

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Classifications MeSH