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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03498781
Other study ID # GFHNRC408
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date April 25, 2018
Est. completion date November 21, 2018

Study information

Verified date January 2022
Source USDA Grand Forks Human Nutrition Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to explore the effects of an intervention designed to help increase physical activity and decrease screen time.


Description:

The purpose of this study is to investigate attendance, exercise, and screen time habits in fitness center members. Because they are the population under investigation, recruitment will take place via the fitness center facilities. This population is under investigation because much of this population is sedentary and does not exercise at recommended levels, despite access to physical fitness facilities. This research will investigate methods to encourage physical activity in this population.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date November 21, 2018
Est. primary completion date November 21, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Body mass index from 18-45 kg/m2 Exclusion Criteria: - have any medical conditions that prevent participant from safely taking part in physical activity - currently a smoker - are pregnant, breastfeeding, or plan to become pregnant - have visited fitness centers more than eight times in the past two months - exercise outside of fitness centers more than once a week for one hour at a time in the past month - do not engage in more than 14 hours a week of screen-based activities - do not have a primarily sedentary job

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise-only
Participants will write goals related to exercise, the most desired outcome of reaching their goals, anticipated obstacles/barriers which may prevent them from achieving their goals, and if-then statements proactively describing how to overcome or avoid obstacles.
Control
Participants will be asked to identify stress-reduction techniques which they can use in their daily lives and will be encouraged to practice them as necessary.

Locations

Country Name City State
United States USDA Grand Forks Human Nutrition Research Center Grand Forks North Dakota

Sponsors (1)

Lead Sponsor Collaborator
USDA Grand Forks Human Nutrition Research Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fitness center attendance Change in fitness center attendance as measured by number of visits per week Week 0, 8, 16
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