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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01067924
Other study ID # 22490
Secondary ID
Status Completed
Phase N/A
First received February 10, 2010
Last updated July 17, 2014
Start date September 2009
Est. completion date August 2013

Study information

Verified date July 2014
Source University of Calgary
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date August 2013
Est. primary completion date April 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility 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

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Motivational interviewing
Intervention arm will receive 2 motivational interviewing session aimed at increasing maintenance of physical activity upon the completion of a supervised exercise program. Motivational interviews will occur at the end of the structured program and at 3 months post program completion. Outcomes will be collected at 6 months post-program.

Locations

Country Name City State
Canada University of Calgary Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
University of Calgary

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in physical activity as measured by the GODIN physical activity questionnaire baseline, 3, 6 months post program No
Secondary Change in Hemoglobin A1C, BMI, six minute walk-test, QoL, and self-efficacy. Baseline, 3, 6 months post-program No
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