Mindfulness-based group intervention for adolescents with type 1 diabetes: initial findings from a pilot and feasibility randomized controlled trial

Author:

Basch Molly12,Lupini Francesca1,Ho Sally1ORCID,Dagnachew Mesgana1,Gutierrez-Colina Ana M34,Patterson Kelly Katherine56,Shomaker Lauren347ORCID,Streisand Randi12ORCID,Vagadori Jack1,Mackey Eleanor12

Affiliation:

1. Center for Translational Research, Children’s National Hospital , Washington, DC, United States

2. Psychiatry & Behavioral Sciences, The George Washington University School of Medicine , Washington, DC, United States

3. Human Development & Family Studies, Colorado State University , Fort Collins, CO, United States

4. Pediatric Endocrinology, University of Colorado Anschutz Medical Campus , Aurora, CO, United States

5. Nursing Science, Professional Practice, & Quality, Children’s National Hospital , Washington, DC, United States

6. Pediatrics, The George Washington University School of Medicine , Washington, DC, United States

7. Pediatric Endocrinology, Children’s Hospital Colorado , Aurora, CO, United States

Abstract

Abstract Objective To evaluate feasibility/acceptability of a virtual, group mindfulness-based intervention (MBI) adapted for pediatric type 1 diabetes (T1D). Methods This two-way controlled trial randomized adolescents 1:1 to MBI (n = 20) or health education (HE; n = 22) groups lasting 6–7 weeks. Eligibility included 12–17 years, T1D ≥ 1 year, and elevated scores on PROMIS depression or anxiety measures. Recruitment, retention, and session attendance were tracked to measure feasibility. Acceptability was measured via youth-reported post-session surveys. Adolescents completed depression, anxiety, and diabetes-specific surveys at baseline, immediately post-program, and 3 months post-program completion. HbA1c values approximating these timeframes were obtained from chart review. Results 55% of screened participants were eligible to participate, and 100% of eligible youth enrolled. There was 93% study retention and 96% session attendance rates. Survey data were 100% complete at baseline, and 93% complete at post-program and 3-month follow-ups; 83% and 78% of MBI participants rated sessions as at least somewhat enjoyable and helpful, respectively, and 91% and 82% of HE participants rated sessions as at least somewhat enjoyable and helpful, respectively. Mean scores showed declines in depression, anxiety, disordered eating, diabetes distress, and HbA1c in both groups across time, with trends toward potential greater reductions in depression and HbA1c in MBI. Conclusions This pilot provides preliminary evidence that virtual MBI and HE groups adapted for adolescents with T1D are feasible to deliver and acceptable, with potential improvement in psychosocial, behavioral, and diabetes-specific outcomes. Whether MBI is more effective for targeting negative affect and glycemic control in the context of adolescent T1D requires testing in a full-scale efficacy trial.

Funder

National Center for Complementary and Integrative Health

Publisher

Oxford University Press (OUP)

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