Skip to main content
Clinical Trials/NCT02746627
NCT02746627CompletedNot Applicable

Positive Psychology to Improve Adherence in Adolescents With Type 1 Diabetes

Vanderbilt University Medical Center1 site in 1 country120 target enrollmentStarted: January 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
120
Locations
1
Primary Endpoint
Glycemic Control (HbA1c)

Study Overview

Brief Summary

Problems with diabetes management in adolescents with type 1 diabetes are common - occurring at rates as high as 93% - and have serious health consequences, including poor blood sugar control and risk for later complications. Therefore, the investigators proposed to test a positive psychology intervention for adolescents with type 1 diabetes aimed at increasing motivation for diabetes management; specifically, to increase the frequency of blood glucose monitoring. This intervention will boost positive mood in adolescents (age 13-17) through tailored exercises in gratitude, self-affirmation, small gifts, and parent affirmation as a way to improve motivation for diabetes management. In addition, this study will explore the use of technology, by comparing telephone-administered vs. automated text-messaging versions of the intervention, to determine which mode of delivery is more appealing, convenient, and beneficial for adolescents in managing their diabetes.

Participants and parents will complete questionnaires on mood and diabetes management during a routine clinic visits at baseline, 3 months, and 6 months. Clinical measures of diabetes management will be collected from participants' electronic medical records.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
13 Years to 17 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Diagnosed with type 1 diabetes for at least 6 months
  • •HbA1c between 8-12%
  • •Speak and read English
  • •Caregiver living with child

Exclusion Criteria

  • •Other uncontrolled health conditions

Arms & Interventions

Education

Active Comparator

Participants receive educational materials in the mail every 2 weeks for 8 weeks.

Intervention: Education (Behavioral)

Positive Affect - Text

Experimental

Participants receive positive affect intervention (weekly reminders to use gratitude, self-affirmations, parental affirmations, and gift cards) by SMS. Participants also receive educational materials in the mail every 2 weeks for 8 weeks.

Intervention: Positive Affect (Behavioral)

Positive Affect - Text

Experimental

Participants receive positive affect intervention (weekly reminders to use gratitude, self-affirmations, parental affirmations, and gift cards) by SMS. Participants also receive educational materials in the mail every 2 weeks for 8 weeks.

Intervention: Education (Behavioral)

Positive Affect - Phone

Experimental

Participants receive positive affect intervention (weekly reminders to use gratitude, self-affirmations, parental affirmations) by phone. Participants receive small gifts in the mail every 2 weeks for 8 weeks. educational materials in the mail every 2 weeks for 8 weeks.

Intervention: Positive Affect (Behavioral)

Positive Affect - Phone

Experimental

Participants receive positive affect intervention (weekly reminders to use gratitude, self-affirmations, parental affirmations) by phone. Participants receive small gifts in the mail every 2 weeks for 8 weeks. educational materials in the mail every 2 weeks for 8 weeks.

Intervention: Education (Behavioral)

Outcomes

Primary Outcomes

Glycemic Control (HbA1c)

Time Frame: 6 months

HbA1c measured as part of diabetes clinic visit. The target for children and adolescents is \<7.5%.

Secondary Outcomes

  • Diabetes-Related Quality of Life(6 months)
  • Family Conflict(6 months)
  • Positive Affect(6 months)
  • Coping(6 months)
  • Frequency of Blood Glucose Monitoring(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sarah Jaser

Assistant Professor

Vanderbilt University Medical Center

Study Sites (1)

Loading locations...

Similar Trials