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A Physical Activity and Diet Program to Prevent Accumulation of Abdominal Fat Mass in Recently Retired Men and Women

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00122213
Recruitment Status : Completed
First Posted : July 21, 2005
Last Update Posted : April 21, 2010
Sponsor:
Collaborator:
Information provided by:

Study Description
Brief Summary:

Advancing age in itself is associated with changes in body composition. However, during transitional life stages, such as retirement, detrimental changes on diet and physical activity may occur. This might lead to weight gain and accumulation of abdominal fat.

To prevent these changes, participants receive a low-intensity intervention on energy balance and related behaviours.

After six months, one and two years, the effects will be studied by comparing the intervention group with the control group.


Condition or disease Intervention/treatment Phase
Retirement Weight Gain Behavioral: Behavior change on physical activity and diet Phase 2

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 400 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: An Individual-based Diet and Physical Activity Intervention Program to Prevent Accumulation of Abdominal Fat Mass in Recently Retired Men and Women
Study Start Date : September 2003
Primary Completion Date : February 2006
Study Completion Date : February 2006

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U.S. FDA Resources

Arms and Interventions


Outcome Measures

Primary Outcome Measures :
  1. Anthropometrics (body weight, height, circumferences, total body fat%, blood pressure)
  2. Energy intake (Food Frequency Questionnaire)
  3. Physical activity level (Physical Activity Scale for the Elderly)

Secondary Outcome Measures :
  1. Psychosocial factors (attitude, social influence, self-efficacy etc.)

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   55 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Apparently healthy and recently retired

Exclusion Criteria:

  • Using drugs that might influence body composition, digestion or physical activities
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00122213


Sponsors and Collaborators
Wageningen University
Netherlands Heart Foundation
Investigators
Study Chair: Evert G Schouten, PhD Wageningen University - Division of Human Nutrition
More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00122213     History of Changes
Other Study ID Numbers: 2000T205
First Posted: July 21, 2005    Key Record Dates
Last Update Posted: April 21, 2010
Last Verified: April 2010

Keywords provided by Wageningen University:
Prevention
Retirement
Physical activity
Diet
Weight gain
Body composition

Additional relevant MeSH terms:
Weight Gain
Body Weight Changes
Body Weight
Signs and Symptoms