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Increasing Heart Healthy Behaviors in Youth With Type 1 Diabetes

Increasing Heart Healthy Behaviors in Youth With Type 1 Diabetes: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03531021
Enrollment
45
Registered
2018-05-21
Start date
2018-05-03
Completion date
2019-02-08
Last updated
2021-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factor, Type1diabetes

Keywords

type 1 diabetes, cardiovascular risk factor, teenager

Brief summary

This study is evaluating how to encourage teens to engage in heart healthy behaviors such as being more active or eating in a healthy way. Teens will be randomly assigned to either the usual care group or the group with education, goal-setting, and lifestyle challenges with teammates.

Detailed description

Specific Aim: To develop and pilot test a modular intervention to improve heart healthy self-efficacy and behaviors in teens with type 1 diabetes at elevated cardiovascular disease risk. Intervention Objective: To evaluate the feasibility and efficacy of a psychoeducational and behavioral intervention to improve heart healthy self-efficacy and behaviors in youth with type 1 diabetes (T1D) at elevated cardiovascular disease (CVD) CVD risk. Secondary Objective: Assess participation in challenges involving healthy eating and physical activity. Synopsis of Study Design Study Design: Randomized, attention-matched trial with 1:1 randomization at a single center. Subjects will be randomized in two strata, by age (14-16 years and 17-19 years). Study Population: Teens with type 1 diabetes. Intervention: This pilot study involves a 6-month randomized controlled trial (RCT) comparing 2 study conditions, the behavioral intervention vs. an attention control. Youth will be randomized in 2 strata, by age (14-16 years and 17-19 years). Enrollment will end after 60 participants. The intervention group will receive 2 modules (one in in person and one by video conference) and will receive follow-up phone calls/emails by study staff 3 weeks following each visit to review education and strategies for and barriers to reaching goals. Intervention sessions must include teen; parents may attend if they wish. Challenges will occur every 2 weeks. Participants will be on teams of about 3-5 teens and the teams may change over the course of the intervention due to staggered enrollment. As team members finish the study, newly randomized teammates will be assigned. There will be a delayed intervention for the control group with study handouts after 3 months. The control group will meet with the research assistants (RAs) for demographic and survey completion and receive reminder phone calls/emails in order to match for attention.

Interventions

BEHAVIORALHeart healthy intervention

Intervention consists of educational modules, goal setting and brainstorming around strategies and barriers, and a series of heart healthy challenges such as walking a certain number of steps or eating healthy foods a certain number of times in a week.

Sponsors

Joslin Diabetes Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Randomized, attention-matched trial with 1:1 randomization at a single center. Subjects will be randomized in two strata, by age (14-16 years and 17-19 years).

Eligibility

Sex/Gender
ALL
Age
14 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* Teens ages 14-19 years old with T1D for ≥6 months * Current patients at Joslin Diabetes Center * Teens will have dyslipidemia (defined as LDL ≥100 mg/dl, HDL \<40 mg/dl or triglycerides ≥130 mg/dl in past year), overweight or obesity (BMI percentile ≥85th at screening), prehypertensive or hypertensive blood pressure on day of screening visit, or A1c ≥8.0% * Youth and parents must be English speaking, without significant learning disabilities, and intend to continue care at our center. * Access to a smart phone with video conferencing capabilities

Exclusion criteria

* Participation in an interventional study within the past 3 months. * Unwilling to comply with study procedures * Prescribed BP and/or lipid-lowering medications (besides over-the-counter supplements) * Contraindication to exercise

Design outcomes

Primary

MeasureTime frameDescription
Adolescent Food Habits Checklist3 monthshealthy eating questionnaire, 23 question true/false survey, score range from 0-23, higher scores indicate healthier habits, no subscales.

Secondary

MeasureTime frameDescription
Blood pressure3 monthsChanges in blood pressure percentile
Changes in lipid levels3 monthsChanges in lipid levels from before study until study end
Activity level3 monthsDocumentation of how active participants were during study
Exercise Confidence Survey3 monthsevaluation of self-efficacy for exercise
Adiposity3 monthschanges in zbmi
Eating Habits Confidence Survey3 monthsevaluation of how confident participants are that they can eat in a healthy way
Acceptance of medication for CVD risk survey3 monthsbrief questions to evaluate willingness to take medication if prescribed
Engagement with behavioral challenges3 monthsProportion of intervention participants who completed challenges
Change in weight3 monthschange in weight in kg between enrollment and study completion
Healthy Eating Self-Efficacy Survey3 monthshealthy eating self-efficacy measure

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026