Viewing Study NCT00399997



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Last Modification Date: 2024-10-26 @ 9:28 AM
Study NCT ID: NCT00399997
Status: UNKNOWN
Last Update Posted: 2006-12-22
First Post: 2006-11-15

Brief Title: Evaluation of Effect of Exercise on Prescription
Sponsor: University of Southern Denmark
Organization: University of Southern Denmark

Study Overview

Official Title: Effect of Exercise on Prescription on Physical Activity Physical Fitness and Health in Patients With Lifestyle Diseases
Status: UNKNOWN
Status Verified Date: 2006-11
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the effect of a primary healthcare intervention called Exercise on Prescription aimed at increasing level of physical activity in a population of sedentary patients with increased risk of developing lifestyle diseases The effect is evaluated using both objective and patient-reported variables
Detailed Description: Exercise prescriptions are used for initiating a physical active lifestyle in sedentary populations

A Danish project called Exercise on Prescription EoP is implemented in primary healthcare Patients eligible for EoP are non-institutionalised adults with medically controlled lifestyle diseases or risk factors of lifestyle diseases who are motivated to change lifestyle able to improve health status through a physical active lifestyle and willing to pay a fee of 100 for the intervention

The purpose of this study is to assess the effect on 1 maximal oxygen uptake VO2max 2 bodyweight and Body Mass Index 3 glycemic control in patients with impaired glucose tolerance 4 physical activity level and 5 health related quality of life

The EoP-group is compared to a control group

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None