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Reducing Stress in Adolescents and Young Adults With Type 1 Diabetes to Improve Diabetes Care (T1D)

Primary Purpose

Type 1 Diabetes

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive Behavioral Therapy
Mindfulness Based Stress Reduction
Diabetes Support and Education
Sponsored by
Wayne State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes focused on measuring insulin dependent diabetes mellitus, adolescents and young adults, stress reduction, metabolic control

Eligibility Criteria

16 Years - 20 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Aged 16 years, 0 months to 20 years, 11 months
  2. Diagnosed with type 1 diabetes for at least six months
  3. Poor metabolic control as defined by HbA1c >=9%

Exclusion Criteria:

  1. Mental health conditions that might compromise data integrity (e.g., developmental delay, psychosis, suicidality)
  2. Co-morbid medical condition resulting in atypical diabetes management (e.g., cystic fibrosis)
  3. Inability to speak or read English

Sites / Locations

  • Wayne State University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Cognitive Behavioral Therapy

Mindfulness Based Stress Reduction

Diabetes Support and Education

Arm Description

Hains' adaptation of cognitive behavioral therapy for adolescents and young adults with type 1 diabetes

Sabinga's adaptation of Mindfulness Based Stress Reduction for adolescents and young adults with type 1 diabetes

Investigator developed peer support group and diabetes education

Outcomes

Primary Outcome Measures

Metabolic Control
Hemoglobin A1c (HbA1c)

Secondary Outcome Measures

Regimen Adherence (objective)
Frequency of Glucose Meter Testing
Regimen Adherence (daily diary)
24 Hour Recall of Diabetes Adherence Behavior
Regimen Adherence (self-reported)
Diabetes Management Scale (DMS)
Psychological Stress (general)
Perceived Stress Scale (PSS)
Psychological Stress (diabetes-related)
Diabetes Stress Questionnaire (DSQ)
Psychological Stress (attitudes)
Hassles and Uplifts Scale
Diabetes Quality of Life
Diabetes Quality of Life Scale

Full Information

First Posted
April 28, 2016
Last Updated
May 31, 2017
Sponsor
Wayne State University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT02760303
Brief Title
Reducing Stress in Adolescents and Young Adults With Type 1 Diabetes to Improve Diabetes Care
Acronym
T1D
Official Title
Reducing Stress in Adolescents and Young Adults With T1D to Improve Diabetes Care
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
September 2015 (Actual)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
May 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wayne State University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Adolescence and young adulthood may be particularly stressful developmental periods due to the numerous transitions into new roles and the need for increased independence. Stress can affect metabolic control in older adolescents and young adults with T1D directly through its impact on cortisol and other hormones that affect insulin metabolism. The proposed study is a pilot randomized clinical trial using a three-group randomized, repeated measures design to assess the efficacy of two treatments (Mindfulness Based Stress Reduction (MBSR) and Cognitive Behavioral Therapy or (CBT) versus an attention control condition for older adolescents and young adults with poorly controlled Type 1 diabetes. As a pilot study, the goal of the research is to test recruitment and retention procedures, finalize intervention measures, training, and fidelity protocols, and estimate effect sizes for a larger clinical trial.
Detailed Description
This study will use a randomized, repeated measures design. A sample of 125 participants will be recruited and consented from the Children's Hospital of Michigan and outpatient diabetes clinics affiliated with the Detroit Medical Center. 108 will be randomized to one of three treatment conditions (remaining participants are expected to consent but not enroll or fail to initiate treatment). These participants will be enrolled in 3 cohorts of 30-36 participants. Measures will be administered at 3 home-based study visits to maximize participant convenience. The initial study visit (Visit 1) will be scheduled at the beginning of the study. Visit 2 will coincide with the end of treatment which is approximately 3 months after the initial study visit. Visit 3 is the 3-month follow up and will be scheduled about 6 months after the initial study visit. At each visit, participants will complete questionnaires assessing their current diabetes management, stressors, quality of life, mental health, and demographic characteristics. These questionnaires will be completed using Qualtrics accessed via the internet on a university laptop computer. A research assistant will download the participant's glucose meter to obtain the frequency of blood glucose testing during the two weeks preceding data collection. The research assistant will also assist participants with providing a blood sample via fingerstick (HbA1c) and saliva samples by mouth (cortisol, Visits 1 and 2 only). All participants will be asked to take part in an exit interview at Visit 3 to obtain feedback on the treatment they received. After Visit 1, participants will be randomized using a 1:1:1 ratio to MBSR, CBT, or Diabetes Support and Education (DSE). All three treatments are group format meeting (10-12 participants per group) for nine consecutive weeks at a location convenient to the participants. In MBSR treatment focuses on the instruction and practice of mindfulness techniques, such as meditation and yoga, and the application of these practices to everyday activities. CBT utilizes activities to understand how thoughts affect emotions and behaviors, the application of these activities to current stressors, and strategies to apply these new skills to future stressors. The DSE group is the attention control condition; DSE participants will receive diabetes education via a support group format. All group sessions will be audiotaped for treatment fidelity monitoring and assessment. There are no planned research interventions for the DSE group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes
Keywords
insulin dependent diabetes mellitus, adolescents and young adults, stress reduction, metabolic control

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive Behavioral Therapy
Arm Type
Experimental
Arm Description
Hains' adaptation of cognitive behavioral therapy for adolescents and young adults with type 1 diabetes
Arm Title
Mindfulness Based Stress Reduction
Arm Type
Experimental
Arm Description
Sabinga's adaptation of Mindfulness Based Stress Reduction for adolescents and young adults with type 1 diabetes
Arm Title
Diabetes Support and Education
Arm Type
Active Comparator
Arm Description
Investigator developed peer support group and diabetes education
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavioral Therapy
Other Intervention Name(s)
CBT
Intervention Description
Participants will attend group therapy sessions, once a week for 9 weeks. The focus of these sessions will be the thought-emotion-behavior linkages as outlined by cognitive-behavioral theory. Activities will illustrate how thoughts affect emotions and behaviors, the application of these activities to current stressors, and strategies to apply these new skills to future stressors.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Based Stress Reduction
Other Intervention Name(s)
MBSR
Intervention Description
Participants will attend group therapy sessions, once a week for 9 weeks. The focus of these sessions will be understanding how to gain control over one's thoughts and feelings using relaxation, meditation, and other mindfulness-based techniques. Activities will focus on the instruction and practice of mindfulness techniques, such as meditation and yoga, and the application of these practices to everyday activities.
Intervention Type
Behavioral
Intervention Name(s)
Diabetes Support and Education
Other Intervention Name(s)
DSE
Intervention Description
Participants will attend group therapy sessions, once a week for 9 weeks. Participants will receive diabetes education via a support group format. The focus of these sessions will be peer group social support and non-adherence diabetes education topics (e.g., emergency preparedness, smoking and diabetes).
Primary Outcome Measure Information:
Title
Metabolic Control
Description
Hemoglobin A1c (HbA1c)
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Secondary Outcome Measure Information:
Title
Regimen Adherence (objective)
Description
Frequency of Glucose Meter Testing
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Title
Regimen Adherence (daily diary)
Description
24 Hour Recall of Diabetes Adherence Behavior
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Title
Regimen Adherence (self-reported)
Description
Diabetes Management Scale (DMS)
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Title
Psychological Stress (general)
Description
Perceived Stress Scale (PSS)
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Title
Psychological Stress (diabetes-related)
Description
Diabetes Stress Questionnaire (DSQ)
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Title
Psychological Stress (attitudes)
Description
Hassles and Uplifts Scale
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months
Title
Diabetes Quality of Life
Description
Diabetes Quality of Life Scale
Time Frame
Change from Baseline at 3 months, Change from Baseline at 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 16 years, 0 months to 20 years, 11 months Diagnosed with type 1 diabetes for at least six months Poor metabolic control as defined by HbA1c >=9% Exclusion Criteria: Mental health conditions that might compromise data integrity (e.g., developmental delay, psychosis, suicidality) Co-morbid medical condition resulting in atypical diabetes management (e.g., cystic fibrosis) Inability to speak or read English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deborah Ellis, Ph.D
Organizational Affiliation
Wayne State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wayne State University School of Medicine
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Reducing Stress in Adolescents and Young Adults With Type 1 Diabetes to Improve Diabetes Care

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