Reducing Cardiometabolic Risk and Promoting Functional Health in Older Adults With Obesity and Prediabetes
NCT ID: NCT03500640
Last Updated: 2025-03-28
Study Results
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View full resultsBasic Information
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COMPLETED
NA
314 participants
INTERVENTIONAL
2018-03-27
2023-05-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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DPP Plus 30-minute calls
Following the 6-month, 16-session, DPP core program, 30-minute group telephone calls will be implemented. Structured behavioral DPP maintenance sessions with a healthy aging focus occur once-per-month from months 7 to 12, and every-two-months from months 13 to 24.
DPP Intensive: 30-minute calls
Ongoing DPP intervention and behavioral progress review to prevent relapse and improve cardiometabolic and functional health targets as keys to healthy aging.
DPP Minimal 15-minute calls
Following the 6-month, 16-session, DPP core program, 15-minute group telephone calls will be implemented. Social-support sessions occur once-per-month from months 7 to 12, and every-two-months from months 13 to 24.
DPP Support: 15-minute calls
No further behavioral intervention materials provided; phone-contacts for mutual social support and accountability
Interventions
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DPP Intensive: 30-minute calls
Ongoing DPP intervention and behavioral progress review to prevent relapse and improve cardiometabolic and functional health targets as keys to healthy aging.
DPP Support: 15-minute calls
No further behavioral intervention materials provided; phone-contacts for mutual social support and accountability
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Ages 60 and older
* Body mass index (BMI) \>= 27 kg/m2
* Prediabetes defined as Hemoglobin (HbA1c) \>= 5.7 % and \<= 6.4 % or fasting glucose of \>= 100 mg/dL and less than 126 mg/dL (at either screening or baseline visit)
* Access to a telephone (for group calls) and to video-player or computer with Internet (to watch session videos and activity videos)
* Able to travel to one of the community clinics in Southwestern Pennsylvania to participate in the first four in-person intervention sessions and five health assessments at 0, 6, 12, 18, and 24 months
* Has health care provider permission to participate
Exclusion Criteria
* Currently taking glucose lowering medications or weight loss medications
* Weight loss of 9 pounds or more in the last six months
* History of bariatric surgery within the last 2 years
* Permanently confined to wheelchair
* Significant cognitive or psychiatric disability that would preclude participation in normal community-based educational activities
60 Years
ALL
Yes
Sponsors
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
University of Pittsburgh
OTHER
Responsible Party
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Elizabeth Venditti
Associate Professor of Psychiatry and Epidemiology
Principal Investigators
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Elizabeth M Venditti, PhD
Role: PRINCIPAL_INVESTIGATOR
Univ. Pittsburgh School of Medicine-Dept. Psychiatry
Locations
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Univ. Pittsburgh School of Medicine-Dept. Psychiatry
Pittsburgh, Pennsylvania, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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PRO17060604
Identifier Type: -
Identifier Source: org_study_id
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