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Motivational Interviewing to Promote Maintenance of Physical Activity in People With Type 2 Diabetes

Not Applicable
Completed
Conditions
Type 2 Diabetes
Interventions
Behavioral: Motivational interviewing
Registration Number
NCT01067924
Lead Sponsor
University of Calgary
Brief Summary

The purpose of the study is to assess the effectiveness of motivational interviewing in promoting maintenance of physical activity in people with Type 2 diabetes (T2D) upon the completion of a structured exercise program.

Participants with T2D who are new graduates of a supervised exercise program will be randomly assigned to either standard care (SC) or to standard care and in addition, participate in two individual motivational interview (MI) sessions (SC + MI).

The primary outcome will be change in physical activity behavior assessed by the Godin Leisure and Exercise questionnaire. Secondary outcomes will include change in blood glucose control (A1C), BMI, six minute walk-test, QoL, and self-efficacy.

Outcomes will be measured in groups at baseline, end of program, 3 months and 6 months post-program.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
55
Inclusion Criteria
  • a) self-reported physician diagnosed T2D, included are those who are treated with diet alone, oral medication and insulin
  • b) clearance by Living Well clinical staff to exercise through GXT algorithm and triaged to "Keep Going" level class,
  • c) at least 18 years of age,
  • d) ability to read and write in English.
Exclusion Criteria
  • a) insulin therapy that began less than 2 years after T2D diagnosis,
  • b) changes during the previous 2 months in oral hypoglycemic

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Motivational interviewingMotivational interviewing-
Standard of careMotivational interviewing-
Primary Outcome Measures
NameTimeMethod
Change in physical activity as measured by the GODIN physical activity questionnairebaseline, 3, 6 months post program
Secondary Outcome Measures
NameTimeMethod
Change in Hemoglobin A1C, BMI, six minute walk-test, QoL, and self-efficacy.Baseline, 3, 6 months post-program

Trial Locations

Locations (1)

University of Calgary

🇨🇦

Calgary, Alberta, Canada

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