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Regulating Efficacy and Wellness in Diabetes (REWinD)

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Edward McAuley, University of Illinois at Urbana-Champaign
ClinicalTrials.gov Identifier:
NCT01790724
First received: February 11, 2013
Last updated: October 27, 2014
Last verified: October 2014

February 11, 2013
October 27, 2014
January 2013
December 2013   (final data collection date for primary outcome measure)
Physical Activity [ Time Frame: Month 6 ] [ Designated as safety issue: No ]
Change from baseline to month six in physical activity. Participants will wear an accelerometer to measure physical activity.
Same as current
Complete list of historical versions of study NCT01790724 on ClinicalTrials.gov Archive Site
  • Self-efficacy [ Time Frame: Month 6 ] [ Designated as safety issue: No ]
    We will assess changes in self-efficacy by written questionnaires.
  • Executive function [ Time Frame: Month 6 ] [ Designated as safety issue: No ]
    Participants will complete a neuropsychological battery of tasks assessing memory, attention and decision-making at baseline and month six.
  • Self-regulatory strategy use [ Time Frame: Month 6 ] [ Designated as safety issue: No ]
    We will assess changes in self-regulatory strategy use by written questionnaires.
  • Physical function [ Time Frame: Month 6 ] [ Designated as safety issue: No ]
    We will conduct functional fitness testing including tests of balance, strength, mobility and flexibility at baseline and six months.
  • Psychosocial outcomes [ Time Frame: Month 6 ] [ Designated as safety issue: No ]
    We will assess changes in psychosocial function ( e.g. self-esteem; social support; anxiety) by written questionnaires.
Same as current
Not Provided
Not Provided
 
Regulating Efficacy and Wellness in Diabetes
Social Cognitive and Neuropsychological Influences on Physical Activity Behavior in Type II Diabetes

The propose of the study is to test the hypothesis that an eight week program consisting of walking exercise and social cognitive theory based group workshops will increase physical activity adherence six months later in older adults with type 2 diabetes or metabolic syndrome.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
  • Diabetes Type 2
  • Metabolic Syndrome
Behavioral: Walking exercise
  • Experimental: Walking exercise
    Participants will be instructed in safe walking exercise. They will participate in an eight week, tapered, on-site program. Participants will also attend group workshops where they will learn self-regulatory skills such as goal-setting, self-monitoring, barrier trouble-shooting, rewarding, and relapse prevention and recovery.
    Intervention: Behavioral: Walking exercise
  • Active Comparator: Metabolic health education
    Participants will complete an eight-week online metabolic health education course. Topics will include glucose control, insulin, weight management, nutrition, physical activity, eye/kidney/foot health, stress reduction, and doctor-patient communication.
    Intervention: Behavioral: Walking exercise
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
125
May 2014
December 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • adults between the ages of 50-75 years
  • individuals diagnosed with type 2 diabetes or metabolic syndrome (presence of 3 of the 5 criteria)
  • physician consent to participate.

Exclusion Criteria:

  • below age 50 or above age 75 at the beginning of the intervention
  • exercising regularly more than twice per week for the last six months
  • diagnosis of type 1 diabetes mellitus
  • failing the Telephone Interview of Cognitive Status
  • inability to communicate in English
Both
50 Years to 75 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01790724
13146, 1F31AG042232-01A1
No
Edward McAuley, University of Illinois at Urbana-Champaign
University of Illinois at Urbana-Champaign
National Institute on Aging (NIA)
Principal Investigator: Edward McAuley, PhD University of Illinois at Urbana-Champaign
University of Illinois at Urbana-Champaign
October 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP