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Feasibility Trial of a Mindfulness Based Intervention in Youth With Type 1 Diabetes (BREATHE-T1D)

Primary Purpose

type1diabetes

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
BREATHE-T1D
Sponsored by
Children's National Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for type1diabetes

Eligibility Criteria

12 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 12-17y
  • T1D, with at least 1-year duration of illness
  • negative affectivity, defined as clinically elevated scores (T-score >55 indicating at least mild depression/anxiety symptoms on either the PROMIS short form-depression and/or anxiety scales)
  • A1c >7.5%
  • English-speaking

Exclusion Criteria:

  • no cognitive or developmental delays which would interfere with their ability to participate in the study
  • are able and willing to complete questionnaires and intervention via the internet
  • do not have severe depression or active or recent (within the past two months) suicidal ideation
  • have no other serious medical conditions (e.g., cystic fibrosis, cancer).

Sites / Locations

  • Children's National HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

BREATHE-T1D

BREATHE-T1D Health Education

Arm Description

BREATHE-T1D is a 6-week group mindfulness program adapted specifically for teens with type 1 diabetes.

The health education placebo comparator is a 6-week group diabetes-specific education program designed to be informational but not supportive.

Outcomes

Primary Outcome Measures

Percentage enrolled of eligible participants screened per month
Number of enrolled participants per month divided by eligible participants screened per month
Number of weeks to enroll participants to form one cohort
Number of weeks to enroll 10 participants to be randomized 5 per group
Percentage of missing assessment data
Number of data points collected per participant divided by total number of data points expected
Percentage of missed sessions per participant
Number of intervention sessions per participant divided by total number of intervention sessions expected
Satisfaction with intervention program
Satisfaction report by participants
Interventionist adherence to session manuals
Ratings of adherence to manual of program sessions by investigators

Secondary Outcome Measures

Mindful Attention Awareness Scale
Assessed via teen report. Scores are calculated as an average score with a range of 1 (minimum) to 6 (maximum) with higher scores indicating more mindful attention in daily life.
Five-Facet Mindfulness Questionnaire
Assessed via teen report. Scores are calculated as an average score with a range of 1 (minimum) to 5 (maximum) with higher scores indicating more mindfulness.
PROMIS Depression Short Form - Adolescent Report
Scores are calculated as t-scores with higher scores indicating more depressive symptoms. T-scores (range 0-100) over 55 indicate clinically significant depressive symptoms.
PROMIS Anxiety Short Form - Adolescent Report
Scores are calculated as t-scores (range 0-100) with higher scores indicating more anxiety symptoms.T-scores over 55 indicate clinically significant anxiety symptoms.
Diabetes Eating Problems Survey Revised
Teen report with higher scores indicating more disordered eating behaviors with scores over 25 indicating clinically significant problems. Total scores range from 0 to 64 with higher scores indicating more disordered eating behaviors.
UPPS-P Negative Urgency subscale
Teen report on the UPPS-P Negative Urgency subscale with higher scores indicating more likelihood to act impulsively when experiencing a negative mood. Scores are calculated with an average which can range from 1(minimum) to 4 (maximum).
Self-Care Inventory
Teen report on the Self-Care Inventory, a measure of diabetes management with higher scores indicating better self-care for diabetes. Average scores range from 1 (minimum) to 5 (maximum).
Problem Areas in Diabetes - Teen
Teen report on the Problem Areas in Diabetes - Teen with higher scores indicating more distress related to diabetes. Average scores range from 1 (minimum) to 6 (maximum).
Glycemic control
HbA1c is a measure of an average blood glucose level over the past 3 months and will be abstracted from the medical record as it is assessed at each regular diabetes clinic visit. HbA1c typically ranges from 4% to >14%.

Full Information

First Posted
February 15, 2022
Last Updated
April 4, 2022
Sponsor
Children's National Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05268393
Brief Title
Feasibility Trial of a Mindfulness Based Intervention in Youth With Type 1 Diabetes
Acronym
BREATHE-T1D
Official Title
Feasibility Trial of a Mindfulness Based Intervention in Youth With Type 1
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 31, 2022 (Actual)
Primary Completion Date
February 2023 (Anticipated)
Study Completion Date
March 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's National Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Type 1 diabetes (T1D) is one of the most common chronic illnesses of childhood. The involved treatment regimen, including daily insulin administration/pump management, frequent blood glucose checks, and careful track-ing of food intake, places a high-stress burden on patients and their families. Adolescence is a particularly risky time for T1D management given a marked decline in treatment adherence and glycemic control. Over 80% of adolescents with T1D have poor glycemic control (A1c >7.5%), and one significant risk factor is the increase in negative affectivity, including depression and anxiety symptoms, that distinguish adolescents with T1D. Elevated depression and anxiety symptoms affect 40% of teens with T1D. Preliminary data support the notion that negative affectivity contributes to diminished treatment adherence and worsening of glycemic control, partially through the effects of negative affectivity on stress-related behavior such as maladaptive eating behavior (e.g., dietary restriction, uncontrolled eating patterns, and insulin omission for weight control). Unfortunately, there is no gold-standard approach to address the poor glycemic control seen in adolescents with T1D. The creation of novel, targeted interventions, tailored for the developmental needs of adolescents with T1D and the particular burdens of coping with their chronic illness, are needed. Mindfulness-based interventions delivered to adolescents without T1D, including the team's preliminary work in teens with depression and weight-related disorders, have shown promise in treating negative affectivity, maladaptive eating behavior, and health outcomes. A mindfulness-based approach may be well-suited for adolescents with T1D, but given that the mechanisms of association among negative affectivity, stress-related behavior, and self-care are unique to individuals with T1D, interventions must be specifically tailored for this population. The goal of this study is to, therefore, adapt an existing 6-session mindfulness-based intervention, Learning to BREATHE, for use with adolescents with T1D (BREATHE-T1D). The first specific aim of the study is to adapt BREATHE for adolescents with T1D and to adapt a relevant and credible health education comparison curriculum (HealthEd-T1D). The second aim is to carry out a 2-way pilot randomized controlled trial to evaluate the feasibility and acceptability of BREATHE-T1D and HealthEd-T1D. The result of the current study will be a feasible and acceptable mindfulness intervention and comparison curriculum that can be evaluated in an efficacy trial. The multidisciplinary study team contributes complementary areas of expertise in adolescents with T1D, behavioral intervention development, negative affectivity and maladaptive eating behavior, adolescent mindfulness-based intervention, qualitative data analysis, and delivery of behavioral health interventions via telehealth. The study's innovative approach will enable the investigators to establish a feasible/acceptable intervention tailored for adolescents with T1D, leading to a future proposal for a full-scale efficacy trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
type1diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
BREATHE-T1D
Arm Type
Experimental
Arm Description
BREATHE-T1D is a 6-week group mindfulness program adapted specifically for teens with type 1 diabetes.
Arm Title
BREATHE-T1D Health Education
Arm Type
Placebo Comparator
Arm Description
The health education placebo comparator is a 6-week group diabetes-specific education program designed to be informational but not supportive.
Intervention Type
Behavioral
Intervention Name(s)
BREATHE-T1D
Intervention Description
BREATHE-T1D is a mindfulness based intervention adapted from Learning to BREATHE specifically for teens with type 1 diabetes.
Primary Outcome Measure Information:
Title
Percentage enrolled of eligible participants screened per month
Description
Number of enrolled participants per month divided by eligible participants screened per month
Time Frame
Baseline
Title
Number of weeks to enroll participants to form one cohort
Description
Number of weeks to enroll 10 participants to be randomized 5 per group
Time Frame
Baseline
Title
Percentage of missing assessment data
Description
Number of data points collected per participant divided by total number of data points expected
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
Percentage of missed sessions per participant
Description
Number of intervention sessions per participant divided by total number of intervention sessions expected
Time Frame
Immediate post-intervention follow-up
Title
Satisfaction with intervention program
Description
Satisfaction report by participants
Time Frame
Immediate post-intervention follow-up
Title
Interventionist adherence to session manuals
Description
Ratings of adherence to manual of program sessions by investigators
Time Frame
Immediate post-intervention follow-up
Secondary Outcome Measure Information:
Title
Mindful Attention Awareness Scale
Description
Assessed via teen report. Scores are calculated as an average score with a range of 1 (minimum) to 6 (maximum) with higher scores indicating more mindful attention in daily life.
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
Five-Facet Mindfulness Questionnaire
Description
Assessed via teen report. Scores are calculated as an average score with a range of 1 (minimum) to 5 (maximum) with higher scores indicating more mindfulness.
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
PROMIS Depression Short Form - Adolescent Report
Description
Scores are calculated as t-scores with higher scores indicating more depressive symptoms. T-scores (range 0-100) over 55 indicate clinically significant depressive symptoms.
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
PROMIS Anxiety Short Form - Adolescent Report
Description
Scores are calculated as t-scores (range 0-100) with higher scores indicating more anxiety symptoms.T-scores over 55 indicate clinically significant anxiety symptoms.
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
Diabetes Eating Problems Survey Revised
Description
Teen report with higher scores indicating more disordered eating behaviors with scores over 25 indicating clinically significant problems. Total scores range from 0 to 64 with higher scores indicating more disordered eating behaviors.
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
UPPS-P Negative Urgency subscale
Description
Teen report on the UPPS-P Negative Urgency subscale with higher scores indicating more likelihood to act impulsively when experiencing a negative mood. Scores are calculated with an average which can range from 1(minimum) to 4 (maximum).
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
Self-Care Inventory
Description
Teen report on the Self-Care Inventory, a measure of diabetes management with higher scores indicating better self-care for diabetes. Average scores range from 1 (minimum) to 5 (maximum).
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
Problem Areas in Diabetes - Teen
Description
Teen report on the Problem Areas in Diabetes - Teen with higher scores indicating more distress related to diabetes. Average scores range from 1 (minimum) to 6 (maximum).
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up
Title
Glycemic control
Description
HbA1c is a measure of an average blood glucose level over the past 3 months and will be abstracted from the medical record as it is assessed at each regular diabetes clinic visit. HbA1c typically ranges from 4% to >14%.
Time Frame
Baseline, Immediate post-intervention follow up, 3 month follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 12-17y T1D, with at least 1-year duration of illness negative affectivity, defined as clinically elevated scores (T-score >55 indicating at least mild depression/anxiety symptoms on either the PROMIS short form-depression and/or anxiety scales) A1c >7.5% English-speaking Exclusion Criteria: no cognitive or developmental delays which would interfere with their ability to participate in the study are able and willing to complete questionnaires and intervention via the internet do not have severe depression or active or recent (within the past two months) suicidal ideation have no other serious medical conditions (e.g., cystic fibrosis, cancer).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eleanor Mackey, PhD
Phone
202-476-5307
Email
emackey@childrensnational.org
Facility Information:
Facility Name
Children's National Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francesca Lupini, M.S.
Phone
202-713-5929
Email
breathet1d@childrensnational.org

12. IPD Sharing Statement

Plan to Share IPD
No

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Feasibility Trial of a Mindfulness Based Intervention in Youth With Type 1 Diabetes

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