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Clinical Trial Details — Status: Withdrawn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• Status: Withdrawn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• Status: Withdrawn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

• Physical Activity
• Sedentary Lifestyle

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