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

This study has been withdrawn prior to enrollment.
Sponsor:
Collaborators:
American Heart Association
Information provided by (Responsible Party):
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT01435564
First received: September 14, 2011
Last updated: June 18, 2014
Last verified: June 2014
  Purpose

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


Condition Intervention
Sedentary Lifestyle
Physical Activity
Behavioral: Mobile phone
Behavioral: pedometer only

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Innovations in Mobile Phone Based Physical Activity- A Pilot of Clinical Trial in Sedentary Men and Women

Further study details as provided by University of California, San Francisco:

Primary Outcome Measures:
  • Pedometer measured steps [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • 7-Day Physical Activity Recall [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Enrollment: 0
Study Start Date: June 2011
Estimated Study Completion Date: June 2013
Estimated Primary Completion Date: May 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: pedometer Behavioral: pedometer only
Participants in this group will receive only a pedometer.
Experimental: Mobile phone physical activity intervention Behavioral: Mobile phone
Participants in this group will receive both the pedometer and the mobile-phone based physical activity intervention fot three months.
Other Name: Mobile phone based physical activity intervention

  Eligibility

Ages Eligible for Study:   21 Years to 69 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

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)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01435564

Locations
United States, California
University of California, San Francisco
San Francisco, California, United States, 94118
Sponsors and Collaborators
University of California, San Francisco
American Heart Association
Investigators
Principal Investigator: Yoshimi Fukuoka, PhD, RN University of California, San Francisco
  More Information

No publications provided

Responsible Party: University of California, San Francisco
ClinicalTrials.gov Identifier: NCT01435564     History of Changes
Other Study ID Numbers: P0030018, K23NR011454
Study First Received: September 14, 2011
Last Updated: June 18, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, San Francisco:
Mobile phone
Sedentary lifestyle
Physical activity
Prevention
Health Promotion
Exercise
eHealth
Electronic diary

ClinicalTrials.gov processed this record on October 16, 2014