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MPOWERed Messages: Tailored Mobile Messages to Enhance Weight Loss for Teens

Novel Individually Tailored Mobile Messages to Enhance Weight Loss for Teens

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01448551
Enrollment
50
Registered
2011-10-07
Start date
2011-10-31
Completion date
2015-10-31
Last updated
2016-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Obesity, Treatment, Adolescents, Text Messages, Mobile phones, Multidisciplinary

Brief summary

Obesity affects millions of American children and increases their risk of adult obesity, a myriad of serious illnesses, increased healthcare costs, and premature death. It is vital to find ways to reverse this epidemic. Multidisciplinary behavioral weight management programs offer the promise of effectively treating childhood obesity. However, participants in such programs often find it challenging to follow recommended treatment plans and frequently drop out from programs without completing them. The proposed project aims to address these problems through frequent contact with patients between office visits. This interim contact will be achieved by automatically sending tailored messages to the mobile phones of adolescents enrolled in a multidisciplinary weight management program (the MPOWER program), as an adjunct to clinic visits. The investigators hypothesize that program participants who receive the tailored text messages will experience lower attrition rates, increased treatment adherence, and greater weight loss compared to those program participants who do not receive the messages.

Interventions

BEHAVIORALTailored Mobile Messages to Enhance Weight Loss for Teens

For this trial adolescents will be allowed to use their own phone (with reimbursement for any study-related costs), or will be provided with a mobile phone, if requested. Participants will receive messages delivered daily over the course of 20 weeks. The content of the messages will be tailored on participants' responses to the MPOWER enrollment survey and the initial tailoring questionnaire. On school days, all messages will be sent after 3 pm (which is after school hours for most Michigan middle and high schools). Therefore, patients will not need to carry cell phones to school. The tailored messages will utilize various degrees of personalization, adaptation and feedback - including momentary assessments with feedback requiring a text reply from the adolescents.

Sponsors

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* BMI ≥ 95th percentile for sex and age according to CDC growth charts * Enrollment in the MPOWER program * At least one parent willing and able to participate in the MPOWER program with the adolescent * Absence of any major medical illness, disability, or moderate/severe mental disorder (e.g., liver disease, renal failure, cancer, bipolar disorder)

Exclusion criteria

* Presence of any major medical illness, disability, or moderate/severe mental disorder (e.g., renal failure, cancer, bipolar disorder) * Physical, mental, or cognitive handicaps that prevent participation * Chronic use of medications that may affect study outcomes (e.g., Diuretics, oral steroids) * Girls who are pregnant, planning to become pregnant in the next 6 months, lactating, or within 6 months postpartum

Design outcomes

Primary

MeasureTime frame
Session attendanceOver the course of 6 months
Adherence to MPOWER program homework assignmentsOver the course of 6 months
Satisfaction with the MPOWER programAt the completion of 3 months and 6 months in the program
Drop outPrior to completion of the 6 month program

Secondary

MeasureTime frameDescription
Change in body mass indexAfter 3 months and 6 months in the MPOWER program
Change in self-report of the six behaviors targeted in the interventionAfter 3 months and 6 months in the MPOWER programThe behaviors addressed are: Breakfast (self-report, in response to the question, During the last 7days, how many days did you eat breakfast?) Fruits and vegetables (24 hour food recall) Fast food (self-report in response to the question, During the last 7 days, how often did you eat food purchased at a fast food restaurant?) Sugar-sweetened beverages (24 hour food recall) Screen time (self-report in response to questions regarding number of hours of screen time per day on school days and non-school days) Physical activity (self-report using the Fitnessgram Activity log)
Objective measurement of daily participation in moderate to vigorous activityAfter 3 months and 6 months in the MPOWER program
Self-efficacy for achieving MPOWER recommendations for the 6 target behaviorsAfter 3 months and 6 months in the MPOWER program6 monthUsing a self-efficacy scale developed by Resnicow we will measure self-efficacy for consuming breakfast daily, achieving recommended amounts of fruits and vegetables, obtaining 60 to 90 minutes of moderate to vigorous physical activity on most days, limiting fast food consumption to no more than once per week, consuming no more than three 8 oz servings of sugar-sweetened beverages per week, and engaging in no more than 2 hours of screen time per day.
Intrinsic motivation to increase intake of fruits and vegetables and to increase physical activityAfter 3 months and 6 months in the MPOWER programIntrinsic motivation will be measured using the Treatment Self-Regulation Questionnaire for Nutrition and the Treatment Self-Regulation Questionnaire for Physical Activity

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026