Consultations in Adapted Physical Activity on Behaviours in Physical Exercise by Type 2 Diabetics

This study has been completed.
Sponsor:
Collaborator:
National Institut of Prevention and Health Education
Information provided by:
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT00403741
First received: November 24, 2006
Last updated: February 26, 2010
Last verified: February 2010
  Purpose

Assesment the impact of three individuals consultations in adapted physical activity by type 2 diabetics


Condition Intervention
Diabetes Mellitus, Type 2
Behavioral: motivational interviewing

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Official Title: Effects of Individuals Consultations in Adapted Physical Activity on Behaviours in Physical Exercise by Type 2 Diabetics

Resource links provided by NLM:


Further study details as provided by University Hospital, Grenoble:

Primary Outcome Measures:
  • Score on Treatment Self-Regulation Questionnaire(TSRQ)at Treatment Self-Regulation Questionnaire (TSRQ) at 3 months, 9 months and 15 months after assesment's day of the education period.

Secondary Outcome Measures:
  • Modifiable Activity Questionnaire(MAQ)at 3 months, 9 months and 15 months after assesment's day of the education period.
  • Perceveid Competence Scale (PCS)at assesment's day of the education period and at 3 months, 9 months and 15 months after assesment's day of the education period.
  • Interpersonal behaviors scale at assesment's day of the education period and at 3 months, 9 months and 15 months after assesment's day of the education period.
  • Diabetes Quality of Life (DQOL) at assesment's day of the education period and at 15 months after assesment's day of the education period.
  • Diabetes Locus of Control Scale (DLCS)at assesment's day of the education period and at 15 months after assesment's day of the education period.
  • HbA1c et lipid profile at 3 months, 9 months and 15 months after assesment's day of the education period.

Estimated Enrollment: 120
Study Start Date: January 2007
Study Completion Date: July 2009
Primary Completion Date: January 2007 (Final data collection date for primary outcome measure)
  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • type 2 diabetics
  • age < 80 years
  • to be able to read and to understand French
  • to be affiliate national insurance
  • to give a light and read consent

Exclusion Criteria:

  • incapacity to carry out a questionnaire
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00403741

Sponsors and Collaborators
University Hospital, Grenoble
National Institut of Prevention and Health Education
Investigators
Principal Investigator: HALIMI SH Serge, PU-PH University Hospital, Grenoble
  More Information

No publications provided

Responsible Party: HALIMI Serge, Professor, University Hospital, Grenoble
ClinicalTrials.gov Identifier: NCT00403741     History of Changes
Other Study ID Numbers: 0621
Study First Received: November 24, 2006
Last Updated: February 26, 2010
Health Authority: France: Ministry of Health

Keywords provided by University Hospital, Grenoble:
behavior
physical activity
motivation

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Endocrine System Diseases
Glucose Metabolism Disorders
Metabolic Diseases

ClinicalTrials.gov processed this record on October 30, 2014