Promoting Resilience in Stress Management for Adolescents With Type 1 Diabetes: A Randomized Clinical Trial.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 Aug 2024
Historique:
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 19 8 2024
Statut: epublish

Résumé

Type 1 diabetes (T1D) requires demanding self-management health behaviors, and adolescents with T1D are at risk for poor psychosocial and medical outcomes. Developing resilience skills may help adolescents with T1D and elevated distress navigate common stressors and achieve positive outcomes. To test the efficacy of the Promoting Resilience in Stress Management (PRISM) intervention on levels of hemoglobin A1c (HbA1c), diabetes distress, self-management behaviors, resilience, and quality of life among adolescents. This phase 3, parallel, 1:1 randomized clinical trial that followed up 172 participants for 12 months was conducted from January 1, 2020, to November 30, 2022, at each of 2 children's hospitals, in Seattle, Washington, and Houston, Texas. Participants were ages 13 to 18 years with T1D for at least 12 months and elevated diabetes distress. PRISM, a manualized, skills-based, individual intervention program that teaches stress management, goal setting, reframing, and meaning-making, facilitated by a coach and accompanied by a digital app, was delivered in three 30- to 60-minute sessions approximately 2 weeks apart. The 2 primary outcomes, diabetes distress and HbA1c levels, and 3 secondary outcomes, resilience, quality of life, and engagement in self-management behaviors, were assessed at baseline and 6 and 12 months after baseline. Linear mixed-effects regression models were used to evaluate associations between PRISM or usual care (UC) and these outcomes at both time points for the intention-to-treat population. Among 172 adolescents (mean [SD] age, 15.7 [1.6] years), 96 were female (56%), and their baseline mean (SD) HbA1c level was 8.7% (2.0%). No differences were evident between PRISM and UC recipients in HbA1c levels (β, -0.21 [95% CI, -0.65 to 0.22]; P = .33) or diabetes distress (β, -2.71 [95% CI, -6.31 to 0.90]; P = .14) or any participant-reported outcome (eg, β, 2.25 [95% CI, -0.30 to 4.80]; P = .08 for self-management behaviors) at 6 months. At 12 months, there was no statistically significant difference between arms in HbA1c levels (β, -0.26 [95% CI, -0.72 to 0.19]; P = .25); however, PRISM recipients reported significantly greater amelioration of diabetes distress (β, -4.59 [95% CI, -8.25 to -0.94]; P = .01) and improvement in self-management behaviors (β, 3.4 [95% CI, 0.9 to 5.9]; P = .01) compared with UC recipients. The findings in this randomized clinical trial of psychosocial and behavioral improvements associated with PRISM at 12 months illustrate the value of a strengths-based intervention. Integrating resilience skills-building with traditional diabetes care may be a promising approach for improving outcomes among adolescents with T1D and elevated diabetes distress. ClinicalTrials.gov number: NCT03847194.

Identifiants

pubmed: 39158914
pii: 2822401
doi: 10.1001/jamanetworkopen.2024.28287
doi:

Substances chimiques

Glycated Hemoglobin 0

Banques de données

ClinicalTrials.gov
['NCT03847194']

Types de publication

Journal Article Randomized Controlled Trial Clinical Trial, Phase III

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2428287

Auteurs

Joyce P Yi-Frazier (JP)

Center for Clinical & Translational Research, Seattle Children's Research Institute, Seattle, Washington.
Department of Psychosocial Oncology & Palliative Care, Dana-Farber Cancer Institute, Boston, Massachusetts.

Marisa E Hilliard (ME)

Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston.

Maeve B O'Donnell (MB)

Center for Clinical & Translational Research, Seattle Children's Research Institute, Seattle, Washington.
Cambia Palliative Care Center of Excellence, University of Washington School of Medicine, Seattle.

Chuan Zhou (C)

Center for Child Health, Behavior, and Development, Seattle Children's Research Institute, Seattle, Washington.
Division of General Pediatrics, Department of Pediatrics, University of Washington School of Medicine, Seattle.

Britney M Ellisor (BM)

Center for Clinical & Translational Research, Seattle Children's Research Institute, Seattle, Washington.

Samantha Garcia Perez (S)

Center for Clinical & Translational Research, Seattle Children's Research Institute, Seattle, Washington.

Brenda Duran (B)

Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston.

Yuliana Rojas (Y)

Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston.

Faisal S Malik (FS)

Center for Child Health, Behavior, and Development, Seattle Children's Research Institute, Seattle, Washington.
Division of Diabetes/Endocrinology, Department of Pediatrics, University of Washington School of Medicine, Seattle.

Daniel J DeSalvo (DJ)

Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston.

Catherine Pihoker (C)

Center for Clinical & Translational Research, Seattle Children's Research Institute, Seattle, Washington.
Division of Diabetes/Endocrinology, Department of Pediatrics, University of Washington School of Medicine, Seattle.

Miranda C Bradford (MC)

Core for Biostatistics, Epidemiology and Analytics for Research (BEAR), Seattle Children's Research Institute, Seattle, Washington.

Samantha Scott (S)

Center for Clinical & Translational Research, Seattle Children's Research Institute, Seattle, Washington.
Department of Psychology, University of Denver, Denver, Colorado.

Sridevi Devaraj (S)

Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston.

Abby R Rosenberg (AR)

Department of Psychosocial Oncology & Palliative Care, Dana-Farber Cancer Institute, Boston, Massachusetts.
Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH