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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02886871
Other study ID # 2016-03-8609-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2016
Est. completion date December 2016

Study information

Verified date October 2018
Source University of California, Berkeley
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall goal of this study is to test personalized mobile phone-based physical activity interventions among staff members at the University of California, Berkeley. Most physical fitness applications for smartphones and activity trackers use a constant goal for the number of steps each day. However, if the step goals are dynamically adjusted according to past behavior, then the corresponding goals may encourage individuals to increase their physical activity level. This study consists of a randomized controlled trial in which we are assessing the efficacy of two different algorithms for calculating personalized goals for the number of steps each day.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- intent to become physically active

- own an iPhone

- willing to keep the iPhone in pockets during the day

- willing to install and use the intervention app every day for 4 months

- ability to speak and read English.

Exclusion Criteria:

- known medical conditions or physical problems that require special attention in an exercise program

- planning an international trip during the next 4 months, which could interfere with daily server uploads of mobile phone data

- pregnant/gave birth during the past 6 months

- severe hearing or speech problem

- history of an eating disorder

- current substance abuse

- current participation in lifestyle modification programs or research studies that may confound study results

- history of bariatric surgery or plans for bariatric surgery in the next 12 months.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Step Goal Delivery by Smartphone


Locations

Country Name City State
United States University of California, Berkeley Berkeley California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Berkeley

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Daily Steps Taken Per Day 10 weeks
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