- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05356884
Adolescent-mediated Family Diabetes Intervention: American Samoa
An Adolescent-mediated Intervention to Improve Diabetes Prevention and Management in Pacific Islander Families
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Pago Pago, American Samoa
- OLaGA Research Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Adolescent
- 14-17 years of age
- Samoan ethnicity
- Shares a household with a parent, legal guardian, or grandparent with type II diabetes
- Willing and able to consent to participation
- Able to participate in group sessions after school or on Saturday mornings
Adult
- Samoan ethnicity
- Diagnosed with type II diabetes at least 12 months prior to study enrollment
- HbA1c >= 6.5%
- Prescribed medication (tablets or insulin) to control their diabetes
- Willing and able to consent to participation
- Willing and able to consent to adolescent's participation
Exclusion Criteria:
Adolescent
- Planning to become pregnant during the study period (any adolescent who becomes pregnant will be excluded from analysis)
- Planning to leave American Samoa in the next 18 months
Participants will be excluded if they report any of the following:
- Uncontrolled hypertension (systolic >180 mmHg or diastolic >105 mmHg)
- Heart attack, stroke, or transient ischemic attack in the past year
- Treatment for cancer
- Chest pain or shortness of breath with minimal activity
- Chronic lung disease, or asthma requiring home oxygen therapy
- Contraindications to moderate physical activity
- Inability to read/speak Samoan and/or English.
- Overt diabetes (HbA1c ≥6.5%) based on point-of-care testing during the screening process
Adult
- Planning to become pregnant during the study period (any adult who becomes pregnant will be excluded from analysis)
- Planning to leave American Samoa in the next 18 months
Participants will be excluded if they report any of the following:
- Uncontrolled hypertension (systolic >180 mmHg or diastolic >105 mmHg)
- Heart attack, stroke, or transient ischemic attack in the past year
- Treatment for cancer
- Chest pain or shortness of breath with minimal activity
- Chronic lung disease, or asthma requiring home oxygen therapy
- Contraindications to moderate physical activity
- Inability to read/speak Samoan and/or English.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Diabetes Intervention
12-session behavioral intervention covering diabetes pathology, self-monitoring, medication adherence, identifying and responding to emergency situations, diet, physical activity, health care utilization and maintaining healthy habits.
|
A 12-session group-based intervention that will target diabetes knowledge and leadership and communication skills through facilitated discussion and experiential learning.
|
|
Active Comparator: Leadership & Life Skills
12-session leadership and life skills intervention focusing on adolescent self-esteem, self-efficacy, communication skills, mindfulnesss, healthy habits.
|
A 12-session group based intervention that will teach leadership and life skills (planning strategies, leadership values, emotional awareness, effective reasoning skills)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Adult Glycemic Control (HbA1c) 0-6 months
Time Frame: 0 - 6 months
|
Glycated hemoglobin (marker of long term glycemic control)
|
0 - 6 months
|
|
Change in Adult Glycemic Control (HbA1c) 0-12 months
Time Frame: 0 - 12 months
|
Glycated hemoglobin (marker of long term glycemic control)
|
0 - 12 months
|
|
Change in Adult Glycemic Control (HbA1c) 6-12 months
Time Frame: 6 - 12 months
|
Glycated hemoglobin (marker of long term glycemic control)
|
6 - 12 months
|
|
Change in Adult Body Mass Index (BMI) 0-6 months
Time Frame: 0 - 6 months
|
Body mass index (measure of weight control)
|
0 - 6 months
|
|
Change in Adult Body Mass Index (BMI) 0-12 months
Time Frame: 0 - 12 months
|
Body mass index (measure of weight control)
|
0 - 12 months
|
|
Change in Adult Body Mass Index (BMI) 6-12 months
Time Frame: 6 - 12 months
|
Body mass index (measure of weight control)
|
6 - 12 months
|
|
Change in Adult Blood Pressure (BP) 0 - 6 months
Time Frame: 0 - 6 months
|
Blood Pressure (marker of hypertension risk)
|
0 - 6 months
|
|
Change in Adult Blood Pressure (BP) 0 - 12 months
Time Frame: 0 - 12 months
|
Blood Pressure (marker of hypertension risk)
|
0 - 12 months
|
|
Change in Adult Blood Pressure (BP) 6 - 12 months
Time Frame: 6 - 12 months
|
Blood Pressure (marker of hypertension risk)
|
6 - 12 months
|
|
Change in Adult Waist Circumference (WC) 0 - 6 months
Time Frame: 0 - 6 months
|
Waist circumference (measure of weight control)
|
0 - 6 months
|
|
Change in Adult Waist Circumference (WC) 0 - 12 months
Time Frame: 0 - 12 months
|
Waist circumference (measure of weight control)
|
0 - 12 months
|
|
Change in Adult Waist Circumference (WC) 6 - 12 months
Time Frame: 6 - 12 months
|
Waist circumference (measure of weight control)
|
6 - 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Adolescent Glycemic Control (HbA1c) 0 - 6 months
Time Frame: 0 - 6 months
|
Glycated hemoglobin (marker of long term glycemic control)
|
0 - 6 months
|
|
Change in Adolescent Glycemic Control (HbA1c) 0 - 12 months
Time Frame: 0 - 12 months
|
Glycated hemoglobin (marker of long term glycemic control)
|
0 - 12 months
|
|
Change in Adolescent Glycemic Control (HbA1c) 6 - 12 months
Time Frame: 6 - 12 months
|
Glycated hemoglobin (marker of long term glycemic control)
|
6 - 12 months
|
|
Change in Adolescent Body Mass Index (BMI) 0 - 6 months
Time Frame: 0 - 6 months
|
Body mass index (measure of weight control)
|
0 - 6 months
|
|
Change in Adolescent Body Mass Index (BMI) 0 - 12 months
Time Frame: 0 - 12 months
|
Body mass index (measure of weight control)
|
0 - 12 months
|
|
Change in Adolescent Body Mass Index (BMI) 6 - 12 months
Time Frame: 6 - 12 months
|
Body mass index (measure of weight control)
|
6 - 12 months
|
|
Change in Adolescent Blood Pressure (BP) 0 - 6 months
Time Frame: 0 - 6 months
|
Blood Pressure (marker of hypertension risk)
|
0 - 6 months
|
|
Change in Adolescent Blood Pressure (BP) 0 - 12 months
Time Frame: 0 - 12 months
|
Blood Pressure (marker of hypertension risk)
|
0 - 12 months
|
|
Change in Adolescent Blood Pressure (BP) 6 - 12 months
Time Frame: 6 - 12 months
|
Blood Pressure (marker of hypertension risk)
|
6 - 12 months
|
|
Change in Adolescent Waist Circumference (WC) 0 - 6 months
Time Frame: 0 - 6 months
|
Waist circumference (measure of weight control)
|
0 - 6 months
|
|
Change in Adolescent Waist Circumference (WC) 0 - 12 months
Time Frame: 0 - 12 months
|
Waist circumference (measure of weight control)
|
0 - 12 months
|
|
Change in Adolescent Waist Circumference (WC) 6 - 12 months
Time Frame: 6 - 12 months
|
Waist circumference (measure of weight control)
|
6 - 12 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nicola L Hawley, PhD, Yale University School of Public Health
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2000031325
- 1R01DK128277-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
Study protocol has been published and is available at: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0279084
Detailed intervention and control curricula will be available in August 2024 upon completion of data collection.
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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