Addressing Place and People Micro Environments in Weight Loss Disparities

Obese Clinical Trial

— APP-ME  

Official title:

APP-ME: Addressing Place and People MicroEnvironments in Weight Loss Disparities

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03083964
• Other study ID #: 1512254890
• Status: Completed
• Phase: N/A
• Start date: January 18, 2017
• Est. completion date: December 11, 2021

Study information

• Verified date: November 2023
• Source: Indiana University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to A) capture obesogenic cues that occur in daily life, and B) to deliver cue alerts. Investigators hypothesized that A) black women experience more cues, B) racial disparities in obesity are reduced in models that adjust for cues, and C) the priming arm will achieve a weight loss of 2kg or more. Investigators will explore whether racial disparities in weight loss differ between the groups receiving usual care or those receiving cues.

Description:

Aim 1: After participants have been consented over the phone or in clinic, the Research Assistants (RA) will schedule a baseline assessment. Baseline interviewer administered survey questions, assessments, and equipment set-up will be completed in participants' homes to allow a physical environment assessment of the home. Assessments and surveys will be carried out using Research Electronic Data Capture (REDCap; see Resources). The in-home baseline assessment piloted for the proposed study takes 1 to 1.5 hours. Global Positioning System (GPS) locating, accelerometry, bite monitoring, and EMA surveys will operate through the mHealth app over the immediate 2-4 week period. For GPS locating, the mHealth app uses software that identifies and sends the longitude and latitude at the time of EMA response to a secure IU server. Software then determines the address of the location and whether it is the participant's home, work, restaurant, retail store, etc. For messaging, the mHealth app uses "Push Notification" to deliver EMA requests to the device (i.e., smartphone). This bypasses the phone carrier's Short Message Service (SMS) gateway, which is not always reliable or secure. The mHealth app makes sure the messages are delivered and secure. Participants receive a notification and open the application to answer the EMA questions. The database is located in a secure network within Indiana University servers. None of the data are stored inside the smartphone at rest. The actual questions are very brief with radio button responses.

At the end of the 2-4 week window, RAs will return to the home to collect the accelerometer and bite counter which takes about 1 hour. The accelerometer and bite counter are to be marked by the RA with the study participants ID and data are retrieved. At this time, participants who responded to 75% or more of the messages over the 2-4 week period, will be randomized to Usual Care (UC) or Priming Arm for Aim 2 and given instruction on the next steps of study participation. Randomization will be carried out within each race group to ensure a balance in the number of subjects between the two treatment arms. The Investigator will computer-generate randomization lists in field envelopes to be provided to the RAs for treatment assignment.

Aim 2: The second aim of the study will last 6 months. Both UC and Priming arms will have full access to Healthy-Me coaches and classes as well as receive training and access to the mHealth app. When study participation is excluded, all apps and associated data will be removed from the smartphone. At no time will Patient Health Information (PHI) be stored on the smartphone. Smartphones will only be identified by study ID number and the developer will only have access to the participants' study ID number and smartphone data collected by the mHealth app. Subjects in UC and Priming will undergo similar assessments and procedures; however, the Priming arm participants will, in addition receive 6-8 message alerts per day. The application and notifications that will be used in the Priming arm will be built from each participants own library to be delivered at times and in locations that their Aim 1 data indicate they often experience an eating or sedentary cue. In short, this intervention counters an obesogenic cue with a "healthy" prime in real-time and location.

Finally, following 6 months of UC or Priming, blinded RAs will return to participants home to complete 6-month follow-up assessment and collect all study related equipment. The final assessment and surveys will take about 1-1.5 hours and all data captured will also be carried out in REDCap.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 350
• Est. completion date: December 11, 2021
• Est. primary completion date: December 11, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 35 Years to 64 Years

Eligibility

Inclusion Criteria:

• Electronic Screener Data (EMR):

1. Aged 35 to 64 years.

2. Female.

3. BMI = 30.

4. Healthy-Me referral or Eligible for Healthy-Me

Self-reported Screener Data:

5. English as primary language.

6. Self-identified non-Hispanic black or African-American, or non-Hispanic white.

7. A permanent address.

Exclusion Criteria:

• Electronic Screener Data (EMR):

1. Severe illness that might be associated with weight loss, such as cancer.

2. Use of weight loss medications (rare due to cost of the medications).

3. History of bipolar disorder or psychosis.

Self-reported Screener Data:

4. Severe cognitive impairment (=3 errors on a 6-item cognitive screen).

5. Unwilling or unable to provide informed consent.

6. Bariatric surgery already completed or planned within 12 months.

7. Pregnant or nursing in past 6 months, or plans to become so within 12 months.

8. Residence outside of Marion County, Indiana.

9. Substance abuse (for alcohol; =2 on CAGE questionnaire).

10. Current smoking or tobacco use.

Related Conditions & MeSH terms

• Obese
• Weight Loss

Intervention

Behavioral:
• Usual Care
Usual care is not considered an intervention. This arm of the study involves a lifestyle coaching intervention delivered in primary care sites to the subjects.
• Priming
The intervention is a just in time eating or physical activity reminder. Each individual participant reports physical activity goals as well as times that they most often eat. This information is used to select for that individual the best time to send an eating or physical activity reminder. The reminders come to the participant's smartphone or a study provided smartphone. Participants will receive reminder 2 to 4 times per day depending on their goals and behavior pattern.

Locations

Country	Name	City	State
United States	Daniel Clark	Indianapolis	Indiana

Sponsors (1)

Lead Sponsor	Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of participants that lose 2 kilograms of weight between baseline and 6 month follow-up	Participants are weighed at baseline and 6 months to access if proportion is losing 2kg of body weight or more by 6 months.	baseline and 6 months
Secondary	Physical activity frequency	Outcomes include ecological momentary assessments that query up to 12 times per day to address physical activity using smartphones.	6 months
Secondary	Eating Frequency	Participants will self-report eating behavior for 3 week periods at baseline and follow-up at 6 month.	6months
Secondary	Depression	Depression is measured using the patient health questionnaire PHQ-4	6 months
Secondary	Anxiety	Anxiety is measured using the patient health questionnaire PHQ-4	6 months