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NCT01435564 Clinical Trial

Pilot Study: Mobile Phone Based Physical Activity in Sedentary Men and Women

Physical Activity Clinical Trial

Official title:
Innovations in Mobile Phone Based Physical Activity- A Pilot of Clinical Trial in Sedentary Men and Women

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01435564
Other study ID # P0030018
Secondary ID K23NR011454
Status Withdrawn
Phase N/A
First received September 14, 2011
Last updated June 18, 2014
Start date June 2011
Est. completion date June 2013

Study information
Verified date June 2014
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this pilot study is to estimate the efficacy of a mobile phone based physical activity intervention in sedentary men and women.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date June 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years to 69 Years
Eligibility Inclusion Criteria:

1. Sedentary lifestyle at work and/or during leisure time

2. Male or female, age between 21-69

3. Access to a telephone at home or a mobile phone

4. Speak and read English

5. BMI between 20-43 kg/m2

Exclusion Criteria:

1. Known medical condition or other physical problems that need special attention in an exercise program

2. Planning a trip out of the United States during the study

3. Pregnant/Delivered a baby during the last 6 months

4. HIV positive

5. Known severe hearing or speech problems

6. Currently participating in lifestyle modification programs or research studies (such as physical activity, diet, and/or weight loss programs)

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Behavioral:
• Mobile phone
Participants in this group will receive both the pedometer and the mobile-phone based physical activity intervention fot three months.
• pedometer only
Participants in this group will receive only a pedometer.

Locations
Country Name City State
United States University of California, San Francisco San Francisco California

Sponsors (3)
Lead Sponsor Collaborator
University of California, San Francisco American Heart Association, National Institute of Nursing Research (NINR)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pedometer measured steps 3 months No
Secondary 7-Day Physical Activity Recall 3 months No
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