Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT05422807 |
Other study ID # |
1R34DK080250 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
April 2011 |
Est. completion date |
July 2016 |
Study information
Verified date |
June 2022 |
Source |
Nemours Children's Clinic |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
This is a randomized, controlled pilot trial of Behavioral Family Systems Therapy for Teens
with Type 2 Diabetes (BFST-DM2), an individual psychological intervention tailored to meet
the needs of teens with type 2 diabetes. It is hypothesized that this behavioral family
intervention will be feasible to implement with teens with type 2 diabetes and will have
positive effects on treatment adherence, health outcomes like weight status and metabolic
control, and psychological outcomes.
Description:
The incidence of type 2 diabetes mellitus (DM2) in youth is increasing dramatically with the
rise in obesity in the U.S. and worldwide. DM2 in youth, as with adults, is clearly linked to
modifiable risk factors such as obesity, sedentary lifestyle, and poor diet. Youth with DM2
are at increased risk for medical complications such as cardiovascular disease, retinopathy,
and neuropathy, as well as psychological problems such as depression, anxiety, poor
self-esteem, eating disorders, and poor coping and problem solving. Although there are
studies demonstrating that family-based lifestyle and psychological interventions are
successful in reducing obesity in youth and in improving metabolic control and adherence in
youth with type 1 diabetes mellitus (DM1), very little has been published on potential
lifestyle or psychological treatments for youth with DM2. Studies have shown that Behavioral
Family Systems Therapy (BFST) has been effective in improving metabolic control, adherence,
family communication, and problem solving in youth with DM1. This intervention could be
effective in treating youth with DM2, as many of the skills necessary for good metabolic
control, health outcomes, treatment adherence, and psychological adjustment are similar in
both populations. This application proposes a randomized, controlled pilot trial of BFST-DM2,
an individual psychological intervention tailored to meet the needs of teens with DM2. BFST
will be adapted to make this intervention more feasible and relevant with minority and
low-income populations and also to focus on weight management, exercise, and nutrition. The
BFST-DM2 intervention includes 12 (90-minute) sessions over 6 months. Areas targeted for
improvement will include metabolic control, weight/body mass index, treatment adherence,
family lifestyle choices (activity, diet), family communication, and problem solving. One of
the main aims of this pilot study is to gather exploratory information on the effectiveness
of the BFST-DM2 intervention on measures of health outcomes, medical adherence, lifestyle
changes, and family problem-solving and communication skills. In addition, it is an aim to
estimate treatment effect size to determine the sample size needed to power a larger
multi-site trial of the BFST-DM2 intervention. Other aims include determining factors
associated with feasibility (recruitment, retention, participation, generalizability) as well
as to modify the intervention to be culturally sensitive and to be more relevant to the
individual needs of the DM2 adolescent population. The BFST-DM2 intervention will be compared
with standard medical therapy on measures of health outcomes (metabolic control, body mass
index, weight, waist circumference, body fat) physical activity (accelerometer), nutritional
intake, treatment adherence, psychological adjustment (self-esteem, quality of life), family
communication, and problem solving. The researchers will analyze predictors of treatment
outcome and the treatment effects at the immediate post-treatment interval (6 months from
baseline). Health outcomes and medical adherence data also will be collected 12 months from
baseline to determine maintenance of treatment effects over time.