Resilient, Empowered, Active Living: REAL Diabetes Study
Status: | Completed |
---|---|
Conditions: | Diabetes, Diabetes, Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 30 |
Updated: | 9/16/2017 |
Start Date: | October 2014 |
End Date: | July 2017 |
Diabetes Self-Management Lifestyle Intervention for Urban Minority Young Adults
This three-year award will pilot-test an innovative intervention, Resilient, Empowered,
Active Living with Diabetes (REAL), targeting underserved minority young adults with
poorly-controlled diabetes. The individually tailored, community-based intervention merges
findings of an in-depth needs assessment, principles of an evidence-based occupational
therapy intervention (Lifestyle Redesign®) and evidence-based diabetes self-management
strategies. A proof-of-concept study demonstrated that REAL is feasible to implement,
acceptable to young adults with type 1 diabetes and type 2 diabetes, and has potential to
produce positive changes in diabetes self-care and glycemic control. The study will randomize
80 young adults with diabetes to receive either the six-month REAL intervention or an
attention control condition. Blinded data collectors will assess glycemic control, diabetes
self-care behaviors and quality of life outcomes, as well as potential intervention
mediators, before and after the six-month intervention. It is anticipated that findings from
this pilot study will be used to inform a large-scale randomized controlled trial of the REAL
intervention.
The study's specific aims and hypotheses are as follows:
Aim 1. Determine the intervention's efficacy for the primary outcomes: glycemic control and
diabetes self-care.
Hypothesis: At 6 months (immediately following the intervention), intervention group
participants will demonstrate improvements in A1C and diabetes self-care as compared to
control group participants.
Aim 2. Conduct exploratory analyses of the intervention's impact on secondary outcomes and
potential mediating mechanisms (to inform power estimates for a large-scale RCT).
Hypothesis 1: At 6 months, intervention group participants will demonstrate improvements in
secondary outcomes: diabetes-related stress and quality of life, depression, and life
satisfaction as compared to control group participants.
Hypothesis 2: At 6 months, intervention group participants will demonstrate improvements in
potential mediators of the intervention: habit strength, problem solving, activity
participation, self-efficacy and diabetes knowledge as compared to baseline.
Aim 3. Conduct a process evaluation utilizing mixed methods to evaluate and refine
intervention delivery (e.g. treatment fidelity, patient satisfaction) and study procedures
(e.g. recruitment, retention, testing protocol).
Active Living with Diabetes (REAL), targeting underserved minority young adults with
poorly-controlled diabetes. The individually tailored, community-based intervention merges
findings of an in-depth needs assessment, principles of an evidence-based occupational
therapy intervention (Lifestyle Redesign®) and evidence-based diabetes self-management
strategies. A proof-of-concept study demonstrated that REAL is feasible to implement,
acceptable to young adults with type 1 diabetes and type 2 diabetes, and has potential to
produce positive changes in diabetes self-care and glycemic control. The study will randomize
80 young adults with diabetes to receive either the six-month REAL intervention or an
attention control condition. Blinded data collectors will assess glycemic control, diabetes
self-care behaviors and quality of life outcomes, as well as potential intervention
mediators, before and after the six-month intervention. It is anticipated that findings from
this pilot study will be used to inform a large-scale randomized controlled trial of the REAL
intervention.
The study's specific aims and hypotheses are as follows:
Aim 1. Determine the intervention's efficacy for the primary outcomes: glycemic control and
diabetes self-care.
Hypothesis: At 6 months (immediately following the intervention), intervention group
participants will demonstrate improvements in A1C and diabetes self-care as compared to
control group participants.
Aim 2. Conduct exploratory analyses of the intervention's impact on secondary outcomes and
potential mediating mechanisms (to inform power estimates for a large-scale RCT).
Hypothesis 1: At 6 months, intervention group participants will demonstrate improvements in
secondary outcomes: diabetes-related stress and quality of life, depression, and life
satisfaction as compared to control group participants.
Hypothesis 2: At 6 months, intervention group participants will demonstrate improvements in
potential mediators of the intervention: habit strength, problem solving, activity
participation, self-efficacy and diabetes knowledge as compared to baseline.
Aim 3. Conduct a process evaluation utilizing mixed methods to evaluate and refine
intervention delivery (e.g. treatment fidelity, patient satisfaction) and study procedures
(e.g. recruitment, retention, testing protocol).
Inclusion Criteria:
- Diagnosed with type 1 or type 2 diabetes mellitus for a minimum of 12 months
- Most recent A1C ≥8.0%
- Fluent in English or Spanish
- Reachable by telephone or text message
- Willing to participate in study activities
- Reside in Los Angeles County with no plans to relocate
Exclusion Criteria:
- Pregnant or planning to become pregnant
- Cognitive impairment or severe disability limiting life expectancy
- Participated in lifestyle intervention targeting diabetes within past 12 months
- Participated in formative research related to intervention development.
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