Home Based Resistance Training For Type 2 Diabetes

This study has been completed.
Sponsor:
Information provided by:
University of Alberta, Physical Education
ClinicalTrials.gov Identifier:
NCT00221208
First received: September 13, 2005
Last updated: March 16, 2009
Last verified: March 2009
  Purpose

This study will investigate the biological and psychosocial benefits of a home-based resistance-training program for sedentary, obese adults living with type 2 diabetes.


Condition Intervention Phase
Diabetes
Behavioral: Resistance Training
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Home Based Resistance Training Program for Obese Adults With Type 2 Diabetes

Resource links provided by NLM:


Further study details as provided by University of Alberta, Physical Education:

Primary Outcome Measures:
  • HbA1c
  • Muscular strength

Secondary Outcome Measures:
  • Fasting blood glucose, insulin, lipid concentrations, C-reactive protein, body composition (DEXA), exercise adherence, behaviour change, psychosocial predictors of resistance training, quality of life.

Estimated Enrollment: 54
Study Start Date: April 2005
Study Completion Date: December 2005
Detailed Description:

Obese individuals with type 2 diabetes will be randomly assigned to either an experimental group where they will perform moderate to high intensity resistance training (50-60% 1RM weeks 1-3 and 70-85% 1RM in weeks 4-16) three times per week for 16 weeks or to a non-training control group. All resistance training will be performed at home using a multigym apparatus. A personal trainer (PT) will come to the homes of each participant in the experimental group to make sure that exercises are being performed safely with the correct technique, and at the prescribed intensity. In the first two weeks, the PT will come to all 3 sessions per week. In weeks 3-4 this will be reduced to 2 times per week, in weeks 5-8 the PT will come once per week and in the last 8 weeks once bi-weekly.

  Eligibility

Ages Eligible for Study:   25 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Type 2 Diabetes Overweight and Obese (BMI>28) Living inside of City limits

Exclusion Criteria:

Ischemic heart disease Osteoporosis Musculoskeletal abnormalities Currently performing resistance training

  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: NCT00221208

Locations
Canada, Alberta
University of Alberta
Edmonton, Alberta, Canada, T6G 2H9
Sponsors and Collaborators
University of Alberta, Physical Education
Investigators
Principal Investigator: Ron C Plotnikoff, PhD University of Alberta
  More Information

No publications provided by University of Alberta, Physical Education

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00221208     History of Changes
Other Study ID Numbers: OHP - 69441
Study First Received: September 13, 2005
Last Updated: March 16, 2009
Health Authority: Canada: Canadian Institutes of Health Research

Keywords provided by University of Alberta, Physical Education:
Diabetes
Resistance Training

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

ClinicalTrials.gov processed this record on September 16, 2014