Quincy Family, Youth & Technology For Lifestyle Change (FYT-4-LIFE) Study

NCT ID: NCT02324361

Last Updated: 2020-10-22

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-07-31

Study Completion Date

2015-02-28

Brief Summary

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To date, approaches that show the most promise for preventing and/or reversing the course of childhood obesity involve the delivery of intensive lifestyle interventions within a family-based context, emphasizing the necessity of parental involvement and making changes in family routines and the home environment. Considering that the current demand for pediatric weight management programs far exceed availability, as well as the high attrition rates observed in such programs, there is a great need for more accessible and efficient means of delivering these interventions to reduce the burden of childhood obesity.

The goal of this study is to understand whether text messaging and social media platforms can be leveraged to address the important issue of childhood obesity by engaging parent/guardians in one of these strategies, and whether these strategies produce similar outcomes. No existing study has compared these strategies head-to-head, and the investigators believe that this project will be instrumental in understanding the determinants of success in these strategies and allow us to collect sufficient intelligence to be able to deploy these meaningfully to patients as part of usual care.

Detailed Description

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The goal of this pilot study is to evaluate and compare the feasibility and effectiveness of two platforms, text messaging and Facebook, for delivering an evidence-based, family-centric childhood obesity intervention to parent/guardians of children between the ages of 3-6 with a BMI of 90th percentile and above. The investigators hypothesize that the use of both platforms for delivering a childhood obesity intervention will help establish healthier family routines and be equally engaging and accepted by parent/guardians and children.

The primary aim of this study is to assess the effect of the intervention on:

* Parent/guardian knowledge of healthy family routines (i.e., nutrition, frequency of family meals, child's screen time, bedtime routines, physical activity, and sleep hours) and of parenting strategies that are preventive of child overweight and obesity
* Parent/guardian readiness, confidence, and perceived self-efficacy to make and maintain changes in family routines known to be associated with healthy weight outcomes

The secondary aims of the study are to assess the effect of the intervention on:

* The adoption of healthy family routines and parenting strategies that are preventive of child overweight and obesity
* Daily objective physical activity in the index child by accelerometry (using a physical activity tracking device)
* Index children's BMI percentile, using data collected during regular clinic visits from the electronic medical record
* To assess the level of engagement with the intervention, measured via daily activity tracker wear by the index child, parent/guardian views of Facebook posts or responses to 2-way text messages

Conditions

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Pediatric Obesity

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

2-arm interventional study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Participants were given a choice to select one of the two interventions, which were made clear to them. There was no masking of the study.

Study Groups

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Facebook group

The intervention consists of evidence-based information on healthy family routines and parenting strategies adapted for Facebook posts on a private study Facebook group.

Participating parents/guardians will have access to all features of the secret study Facebook group (e.g., create and view postings, comment and like existing posts and view user names of other members of the group (existing study participants and staff) for the duration of the study.

All index children will be provided with a Physical Activity Monitor to wear during waking hours for the duration of the study.

Group Type EXPERIMENTAL

Physical Activity

Intervention Type OTHER

The Fitbit Zip is a wireless physical activity monitor that will be worn by the index child during waking hours, and will be used to assess daily active time for the duration of the study.

Evidence-based information on healthy family routines

Intervention Type BEHAVIORAL

Educational dimensions include nutrition, frequency of family meals, child's screen time, bedtime routines, physical activity, and sleep hours.

Text messaging

The intervention consists of evidence-based information on healthy family routines and parenting strategies adapted for 140-character text messages.

The automated text-messaging algorithm consists of the delivery of two types of text messages: 1-way messages, in which participating parents/guardians will receive a piece of education or motivation on the dimension topic that they're being coached on and 2-way messages, in which participants are able to respond to an educational message containing a number response prompt that will provide them with personalized feedback regarding a dimension they are being coached on.

All index children will be provided with a Physical Activity Monitor to wear during waking hours for the duration of the study.

Group Type EXPERIMENTAL

Physical Activity

Intervention Type OTHER

The Fitbit Zip is a wireless physical activity monitor that will be worn by the index child during waking hours, and will be used to assess daily active time for the duration of the study.

Evidence-based information on healthy family routines

Intervention Type BEHAVIORAL

Educational dimensions include nutrition, frequency of family meals, child's screen time, bedtime routines, physical activity, and sleep hours.

Interventions

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Physical Activity

The Fitbit Zip is a wireless physical activity monitor that will be worn by the index child during waking hours, and will be used to assess daily active time for the duration of the study.

Intervention Type OTHER

Evidence-based information on healthy family routines

Educational dimensions include nutrition, frequency of family meals, child's screen time, bedtime routines, physical activity, and sleep hours.

Intervention Type BEHAVIORAL

Other Intervention Names

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Change in Physical Activity

Eligibility Criteria

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Inclusion Criteria

* Index child's BMI ≥90th percentile
* Index child age between 3 and 7 years of age at time of enrollment in study
* The child is under the care of a primary care provider at the Quincy Pediatric Associates practice
* The family is not planning to move from the Greater Boston area during the study period

The participating parent/guardian:

* Is 18 years or older
* Is the primary caregiver for the child
* Has regular access to the Internet
* Has regular access to a personal computer with USB connection OR a smartphone with a mobile operating system that is compatible with the physical activity tracker
* Owns a Facebook account AND a cellphone with text messaging capability and if choosing the text-messaging intervention, is willing to receive a maximum of 62 text messages/month for 3 months on their personal cellphone
* Is fluent in English (spoken and written)

Exclusion Criteria

* Children who are diagnosed with underlying medical or pharmacologic factors that may contribute to obesity and/or affect participation in physical activity
* Significant medical or psychiatric co-morbidities in the participating parent/guardian
* Visual, hearing, or cognitive impairments in the participating parent/guardian
* Index child or parent/guardian currently enrolled in another weight control program
* Children who have a sibling already enrolled in the study
Minimum Eligible Age

3 Years

Maximum Eligible Age

7 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Massachusetts General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Joseph C. Kvedar

Dermatologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kamal Jethwani, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

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Quincy Pediatric Associates

Quincy, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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2014P000873

Identifier Type: -

Identifier Source: org_study_id

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