The purpose of this study is to see if it is practical to use social media-based and traditional online weight loss intervention components among low socioeconomic status participants using the Facebook social media (SM) and Fitbit self-monitoring platforms. Also, the study will test the effectiveness of recruiting participants via social media and at community events and locations. The results of this study will be used to inform future research studies.
The primary objectives of the proposed research are to: 1. assess the feasibility of social media-based (social support, social competition, and social rewards) and traditional online weight loss (education and goal setting) intervention components delivered to low-Socioeconomic Status (SES) participants using the Facebook SM and Fitbit self-monitoring platforms and 2. develop and assess methods for recruiting and retaining adequate numbers of low-SES participants for a future randomized controlled trial to assess the efficacy of an SM-based weight loss intervention. The study team will assess feasibility by conducting a 12-week pilot test of traditional and social media-based weight loss intervention components followed by qualitative and quantitative assessment with pilot participants. The specific aims are: Aim 1- Assess trial feasibility: The study team will assess intervention processes critical to the success of a larger efficacy trial during the 12-week pilot including: (1) participant recruitment and retention, (2) participant use of intervention components, (3) use of data collection strategies and instruments. Aim 2 - Assess intervention acceptability: The study team will conduct structured interviews and surveys among participants to assess participants' experience during the intervention. This study focuses on: (1) intervention design and content, (2) participant use of intervention technologies (Facebook and Fitbit), (3) participant concerns about privacy, and (4) barriers and facilitators to recruitment, retention, and participation. Findings will be used to improve the design of a larger efficacy trial. Study Design: This study will employ a one group pre-post design.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
55
Fitbit Activity Monitor and IPAQ to give level of physical activity. Participants will be provided with education about physical activity recommendations and will be encouraged to set goals for improvement.
National Cancer Institute's ASA24 web-based dietary assessment tool to determine intake. Participants will be provided with education about healthy diets and will be encouraged to set goals for making enduring changes to dietary intake.
Social support will be determined via self report scale measure and objective collection of social media communications. Each participant will be contacted through social media regularly with dietary and physical activity information and asked to support other participants via encouragement and sharing of information.
Case Western Reserve Univeristy
Cleveland, Ohio, United States
Ratio or participants screened to patients completing 12-week measures
This is a measure of feasibility
Time frame: Up to 12 weeks
Average score of adapted INSHAPE computer-based questionnaire
Computer-based questionnaires will be self-administered via the Qualtrics Survey platform. INSHAPE questionnaire is a 14 question survey gauging acceptability of the program
Time frame: Up to 12 weeks
Number of eligible participants
This is a measure of feasibility
Time frame: Up to 12 weeks
Number of consented participants
This is a measure of feasibility
Time frame: Up to 12 weeks
Average change in Fitbit activity
This is a measure of physical activity
Time frame: From baseline to 12 weeks
Average change in International physical activity questionnaire (IPAQ) score
This is a measure of physical activity
Time frame: From baseline to 12 weeks
Average change in score of the National Cancer Institute's Automated Self-Administered 24-Hour (ASA24) dietary assessment web-based assessment tool
This is a measure of dietary intake
Time frame: From baseline to 12 weeks
Change in weight
Trained study staff will determine weight at baseline and 12 weeks of the study
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Time frame: From baseline to 12 weeks
Change in waist circumference
Trained study staff will determine waist circumference at baseline and 12 weeks of the study
Time frame: From baseline to 12 weeks
Average change in social support score
This is a 31 question, multiple choice survey adapted from Gruber and Sallis
Time frame: From baseline to 12 weeks
Average change in weight loss self-efficacy score
Multiple choice questions and short answer survey which can be scored to gauge weight-loss self-efficacy. Adapted from Wilson
Time frame: From baseline to 12 weeks
Average change in dietary knowledge
Multiple choice questions and short answer survey which can be scored to gauge dietary knowledge. Adapted from Jones
Time frame: From baseline to 12 weeks