mHealth Messages to Sustain Recent Weight Loss - Phase 2
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02279017|
Recruitment Status : Completed
First Posted : October 30, 2014
Last Update Posted : January 26, 2017
To assess the feasibility to translate an automated weight loss message intervention to a weight loss clinic population.
Aim 1: To assess feasibility of translating the intervention in a clinic for patients who recently completed a structured weight loss program.
Aim 2: To assess the ability to capture a trajectory of self-reported weight over 6 months through an automated intervention.
|Condition or disease||Intervention/treatment||Phase|
|Weight Loss||Behavioral: mHealth Texting for Weight Loss||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||100 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Basic Science|
|Official Title:||Mobile Health Messages to Sustain Recent Weight Loss - Phase 2|
|Actual Study Start Date :||October 2014|
|Actual Primary Completion Date :||January 2017|
|Actual Study Completion Date :||January 2017|
We will send the study participate a daily text message for 2 months to their phone at 8 A.M. and a weekly text message for 6 months asking them to report their weight through a 2-question online survey. After that, a monthly text message for 18 months asking them to report their weight.
Behavioral: mHealth Texting for Weight Loss
- Subject's weight loss [ Time Frame: 2 years ]The study is being done to asses the ability to translate an automated weight loss message intervention to a weight loss clinic population.
- Percentage of subjects who self-report weight to the clinic [ Time Frame: 2 years ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02279017
|United States, North Carolina|
|Duke University Medical Center, Diet and Fitness Center|
|Durham, North Carolina, United States, 27710|
|Principal Investigator:||Ryan Shaw, RN, Phd||Duke University|