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Clinical Trials/NCT01377506
NCT01377506CompletedNot Applicable

Translation of Obesity and Cognitive Research in a Rural State Via Senior Centers

University of Arkansas0 sites16 target enrollmentStarted: September 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
16
Primary Endpoint
weight loss

Study Overview

Brief Summary

Obesity is a major public health problem among older adults, with 31% of non-institutionalized older persons (60 years+) in the US obese and projections indicating that this will rise to 40% by 2010. A second public health challenge on the horizon for the aging US population is the increasing number of individuals experiencing cognitive decline, dementia or Alzheimer 's disease. Recent clinical trials have demonstrated efficacy in reducing risks associated with both of these significant and increasingly pervasive health problems, which are more common among rural, low income and ethnic minority populations. The Diabetes Prevention Program (DPP) Lifestyle Intervention produced sustained weight losses in a large, diverse population of high-risk individuals and dramatically reduced rates of type 2 diabetes onset, particularly among older adults. SeniorWISE produced improvements in memory in community dwelling older persons. Transferring these exciting technologies to community settings where they can benefit older adults is a pressing public health need. Therefore, the current project seeks to transfer these two evidence-based interventions to older adults in a rural state using senior centers as the venue for dissemination and lay health educators to deliver the interventions. Senior centers are a particularly attractive context for translation of evidence-based health promotion technologies in predominantly rural states like Arkansas because they have a well-established infrastructure in communities and share a common goal of promoting healthy aging and reducing health care costs. The 3-year randomized, controlled trial will evaluate translation of the interventions by randomizing senior centers (N=16) across Arkansas to implement either (1) the DPP Lifestyle Weight Loss Program or (2) the SeniorWISE Cognitive Training Program. Older (age > 60) adults (N=288) nested within senior centers will receive the programs delivered in a group format by a trained lay health educator. Primary outcomes are changes in body weight and cognitive functioning at 12 months. The multi-level evaluation plan will characterize reach, effectiveness, adoption, implementation and maintenance of the interventions, with a cost effectiveness component.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •for senior centers (unit of randomization):
  • •located in the state of Arkansas
  • •agree to be randomized
  • •able to identify two or three volunteers or staff members willing to be trained (including IRB certification) and deliver the programs within the senior center over the course of a year
  • •have adequate space for group meetings and for private data collection visits
  • •agreement that it would be likely that they could identify 18 interested and eligible (obese and not cognitively impaired) senior adults willing to attend the program over the course of 12 months

Exclusion Criteria

  • •inability to identify and secure lay health educator from within their community
  • •concerns of inability to recruit the requisite 18 senior adult participants who met minimal inclusion criteria

Arms & Interventions

Lifestyle counseling

Experimental

Diabetes Prevention Program Lifestyle Balance Intervention delivered by lay health educator

Intervention: lifestyle counseling (Behavioral)

Cognitive Training

Active Comparator

Adaptation of SeniorWise Memory Training program for delivery by lay health educator, matched in duration and contact to the other study arm

Intervention: Cognitive Training (Behavioral)

Outcomes

Primary Outcomes

weight loss

Time Frame: 4 and 12 month

weight change from baseline in kg and percent weight loss \[1-(12-month weight/baseline weight)

Secondary Outcomes

  • cognitive function(4 and 12 month)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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