Pilot Study: Mobile Phone Based Physical Activity in Sedentary Men and Women
Innovations in Mobile Phone Based Physical Activity- A Pilot of Clinical Trial in Sedentary Men and Women
2 other identifiers
interventional
N/A
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Jun 2011
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2011
CompletedFirst Submitted
Initial submission to the registry
September 14, 2011
CompletedFirst Posted
Study publicly available on registry
September 16, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2013
CompletedJune 19, 2014
June 1, 2014
1.9 years
September 14, 2011
June 18, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pedometer measured steps
3 months
Secondary Outcomes (1)
7-Day Physical Activity Recall
3 months
Study Arms (2)
pedometer
ACTIVE COMPARATORMobile phone physical activity intervention
EXPERIMENTALInterventions
Participants in this group will receive both the pedometer and the mobile-phone based physical activity intervention fot three months.
Eligibility Criteria
You may qualify if:
- Sedentary lifestyle at work and/or during leisure time
- Male or female, age between 21-69
- Access to a telephone at home or a mobile phone
- Speak and read English
- BMI between 20-43 kg/m2
You may not qualify if:
- Known medical condition or other physical problems that need special attention in an exercise program
- Planning a trip out of the United States during the study
- Pregnant/Delivered a baby during the last 6 months
- HIV positive
- Known severe hearing or speech problems
- Currently participating in lifestyle modification programs or research studies (such as physical activity, diet, and/or weight loss programs)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of California, San Franciscolead
- American Heart Associationcollaborator
- National Institute of Nursing Research (NINR)collaborator
Study Sites (1)
University of California, San Francisco
San Francisco, California, 94118, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yoshimi Fukuoka, PhD, RN
University of California, San Francisco
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 14, 2011
First Posted
September 16, 2011
Study Start
June 1, 2011
Primary Completion
May 1, 2013
Study Completion
June 1, 2013
Last Updated
June 19, 2014
Record last verified: 2014-06