Mindfulness-based group intervention for adolescents with type 1 diabetes: initial findings from a pilot and feasibility randomized controlled trial.
Molly Basch, Francesca Lupini, Sally Ho, Mesgana Dagnachew, Ana M Gutierrez-Colina, Katherine Patterson Kelly, Lauren Shomaker, Randi Streisand, Jack Vagadori, Eleanor Mackey
Journal of pediatric psychology October 1, 2024 DOI: 10.1093/jpepsy/jsae071 via PubMed
Summary
AI-generated from the abstractA virtual mindfulness-based intervention adapted for adolescents with type 1 diabetes and elevated depression or anxiety symptoms was compared to a health education program in a pilot trial. Among 42 adolescents aged 12–17, 55% of screened youth were eligible and all enrolled. Retention was 93%, session attendance 96%, and survey completion 93% at follow-ups. Both groups showed declines in depression, anxiety, disordered eating, diabetes distress, and HbA1c over time, with trends toward greater reductions in depression and HbA1c in the mindfulness group. The findings suggest both interventions are feasible and acceptable, but a full trial is needed to test whether the mindfulness approach is more effective.
Study at a glance
| Characteristics | Pilot/feasibility trial Randomized Peer reviewed |
|---|---|
| Sample size | 42 |
| Population | Adolescents aged 12–17 with type 1 diabetes for at least 1 year and elevated scores on PROMIS depression or anxiety measures |
| Interventions | Mindfulness-based intervention Health education |
| Duration | 6-7 weeks intervention, 3-month follow-up |
| Topics | Anxiety Depression |
| Keywords | Adolescents Diabetes Pilot/feasibility trial |
| Citations | 8 |
| Key finding | Both the virtual mindfulness-based intervention and health education groups were feasible and acceptable, with trends toward greater reductions in depression and HbA1c in the mindfulness group. |
Abstract
To evaluate feasibility/acceptability of a virtual, group mindfulness-based intervention (MBI) adapted for pediatric type 1 diabetes (T1D). 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. 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. 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.