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Clinical Trials/NCT03847194
NCT03847194
Completed
Not Applicable

The Promoting Resilience in Stress Management (PRISM) Intervention: a Multisite Randomized Control Trial in Adolescents With Type 1 Diabetes

Seattle Children's Hospital2 sites in 1 country172 target enrollmentJanuary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 1 Diabetes Mellitus
Sponsor
Seattle Children's Hospital
Enrollment
172
Locations
2
Primary Endpoint
A1C
Status
Completed
Last Updated
last year

Overview

Brief Summary

It is well-known that adolescents with type 1 diabetes are at high risk for elevated diabetes-specific distress and poor glycemic control. This randomized controlled trial uses a novel, person-centered intervention designed to reduce diabetes distress and improve resilience skills, which the investigators hypothesize will in turn improve glycemic control and quality of life. If successful, results will greatly inform future research and clinical strategies aimed at improving outcomes among adolescents with type 1 diabetes.

Detailed Description

Adolescents with type 1 diabetes (T1D) are at high risk for elevated diabetes distress, which greatly impacts their adherence, glycemic control (A1C), and overall quality of life (QOL). A potential barrier to improving these experiences may be that adolescents have few opportunities to develop the personal resources needed to handle adversity and manage stress. The "Promoting Resilience in Stress Management" (PRISM) intervention is a manualized, brief, skills-based intervention delivered in 2, 45-60 minute one-on-one sessions, followed by a family meeting and supplemented by booster sessions and a digital app. PRISM was developed from Stress and Coping theory and targets skills in stress-management and mindfulness, goal-setting, positive reframing, and meaning-making. All of these skills are associated with improved patient outcomes in diverse groups of adolescent populations with chronic/serious illness, and findings from a feasibility trial in adolescents with T1D showed PRISM to be highly feasible and desirable in this population. Further, a recent pilot randomized controlled trial among adolescents with cancer suggest PRISM is associated with improved perceptions of resilience, lower psychological distress, and higher QOL. This application proposes to build on our prior experience and fill three critical knowledge gaps: (1) PRISM's impact on A1C among adolescents with T1D; and (2) PRISM's impact on diabetes distress, self-reported adherence, and other patient-reported outcomes including resilience and QOL. This funding opportunity seeks to test interventions targeting diabetes distress for impact on glycemic control. Thus, the investigators propose a multi-site randomized controlled trial among N=160 adolescents (n=80 PRISM, n=80 Usual Care; ages 13-18) with the primary trial outcome of glycemic control 6-months post-enrollment. Time-in-range will be evaluated for participants on continuous glucose monitors as an exploratory aim. Secondary outcomes will include diabetes-distress, and patient-reported adherence, resilience, and quality of life. The investigators hypothesize PRISM will promote better glycemic control and improved diabetes distress than usual care. This application offers an opportunity to expand the body of knowledge regarding methodologically rigorous and evidence-based interventions for adolescents with T1D. Ultimately, this research has the potential to offer a practical, skills-based curriculum designed to improve outcomes for this high-risk group.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
March 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Joyce Yi-Frazier

Senior Clinical Research Scientist

Seattle Children's Hospital

Eligibility Criteria

Inclusion Criteria

  • • They are 13-18 years old
  • Diagnosed with T1D \>12 months
  • Elevated distress score (PAID-T\>=30)\*\*\*\*\*
  • Speak English fluently
  • Cognitively able to participate in intervention sessions and complete written surveys.

Exclusion Criteria

  • Patient refusal to participate (any age), or parental refusal to participate for patients less than 18 years of age
  • Cognitively or physically unable to participate
  • Patient unable to speak in the English language
  • Patient unable to read in the English or Spanish language
  • Adolescent is ward of state

Outcomes

Primary Outcomes

A1C

Time Frame: 6 months

hemoglobin A1C

Diabetes Distress

Time Frame: 6 months

Diabetes distress will be measured with the Problem Areas in Diabetes Scale, Teen Version. Higher scores indicate more distress. Total score ranges from 6 to 84.

Secondary Outcomes

  • Diabetes-specific Quality of Life(6 months)
  • Adherence(6 months)
  • Resilience(6 months)

Study Sites (2)

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