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Sustaining the Reach of a Scalable Weight Loss Intervention Through Financial Incentives

Primary Purpose

Overweight and Obesity

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Financial incentives
Sponsored by
University of Nebraska
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight and Obesity focused on measuring Financial incentive, Behavioral economics, Attrition, Reach, Participation, Retention, Weight loss

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Overweight or obese participants who are of 19 years or older and have internet access

Exclusion Criteria:

  • Not meeting the inclusion criteria.

Sites / Locations

  • Nebraska Medicine Fontenelle clinic

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

Weight loss incentive

Weigh-in incentive

Combination incentive

Choice option incentive

Arm Description

Participants will receive incentive rewards based on WEIGHT LOSS outcomes.

Participants will receive incentive rewards based on WEIGH-INs frequency

Participants will receive half of the incentive from WEIGHT LOSS and WEIGH-INs

Participants will choose one out of the three incentive programs (Weight-loss, Weigh-ins, and Combination).

Outcomes

Primary Outcome Measures

Sustaining the reach
Percentage of participants returning to weigh-in 3, 6, and 12 months after initial program registration

Secondary Outcome Measures

Weight loss
weight loss achieved at 3, 6 and 12 months
Clinical meaningful weight loss
Percentage of participants achieving clinically significant weight loss (percentage of patients who lost >3% or >5% of their initial bodyweight)

Full Information

First Posted
January 8, 2020
Last Updated
August 25, 2023
Sponsor
University of Nebraska
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1. Study Identification

Unique Protocol Identification Number
NCT04225234
Brief Title
Sustaining the Reach of a Scalable Weight Loss Intervention Through Financial Incentives
Official Title
Sustaining the Reach of a Scalable Weight Loss Intervention Through Financial Incentives: an Exploratory Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Terminated
Why Stopped
Due to the COVID-19 pandemic
Study Start Date
August 20, 2019 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
August 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nebraska

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study seeks to assess how different incentive strategies may reduce the initial attrition gap when implementing weight management in a primary care clinic predominantly serving African American patients. This will be done through an innovative research-practice partnership involving primary care, research expertise, and a small business. Participants will be randomly assigned to one of four financial incentive conditions respectively tied to: weight loss, weigh-ins, weigh-ins and weight-loss, and incentive choice. Participants will be followed for 3 and 6 months to assess program reach, sustaining the reach after initial weigh-in, and weight loss outcomes based on records on participant enrollment and subsequent weigh-ins automatically collected through a kiosk at the clinic.
Detailed Description
The proposed study "Sustaining the Reach of a Scalable Weight Loss Intervention through Financial Incentives: an Exploratory Randomized Trial" seeks to assess how the use of different incentive strategies may reduce the initial attrition gap when implementing weight management in a primary care clinic predominantly serving African American patients through an innovative research-practice partnership involving primary care, research expertise, and a small business. The sample will include approximately 200 persons ages 19+ from Nebraska Medicine or the greater Omaha community. The inclusion criteria are (1) age 19+ years; (2) are obese (BMI >=30) or overweight (BMI >=25 yet smaller than 30); (3) have internet access. Following the completion of an automated informed consent embedded within the program registration using a kiosk placed at the Fontenelle Clinic, we plan to conduct a 4-arm, pragmatic randomized controlled trial (RCT) that will randomly assign overweight/obese patients at the Nebraska Medicine Fontenelle clinic to one of four financial incentive conditions respectively tied to: weight loss, weigh-ins, weigh-ins and weight-loss, and incentive choice, following the completion of an automated informed consent embedded within the program registration and initial weigh-in. Participants will be followed for 3 and 6 months to assess program reach, sustaining the reach after initial weigh-in, and weight loss outcomes based on records on participant enrollment and subsequent weigh-ins automatically collected through a kiosk placed at the Fontenelle clinic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity
Keywords
Financial incentive, Behavioral economics, Attrition, Reach, Participation, Retention, Weight loss

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Our proposed project would be most appropriately be categorized as a partial factorial with choice model, because our study design includes 2 intervention each alone (weight loss and weigh-in), and in combination (weight loss + weigh-in), and choice. No control group is included.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
119 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Weight loss incentive
Arm Type
Active Comparator
Arm Description
Participants will receive incentive rewards based on WEIGHT LOSS outcomes.
Arm Title
Weigh-in incentive
Arm Type
Experimental
Arm Description
Participants will receive incentive rewards based on WEIGH-INs frequency
Arm Title
Combination incentive
Arm Type
Experimental
Arm Description
Participants will receive half of the incentive from WEIGHT LOSS and WEIGH-INs
Arm Title
Choice option incentive
Arm Type
Experimental
Arm Description
Participants will choose one out of the three incentive programs (Weight-loss, Weigh-ins, and Combination).
Intervention Type
Other
Intervention Name(s)
Financial incentives
Intervention Description
Depending on their level of participation or weight loss outcomes, participants will have the opportunity to receive between $60-$120 (over 12 months), on average, regardless of program assignment. Regardless of which incentive program that participants are randomized to, they will receive the incentaHEALTH weight loss program intervention. incentaHEALTH is an technology-supported multi-component coaching intervention for weight loss includes a website, objective weight assessment using HIPAA-compliant kiosks, daily social cognitive theory-based email and text message support, and online access to health coaches. The intervention encourages increased intake of fruit, vegetables, lean protein, and complex carbohydrates while monitoring portion sizes.
Primary Outcome Measure Information:
Title
Sustaining the reach
Description
Percentage of participants returning to weigh-in 3, 6, and 12 months after initial program registration
Time Frame
3, 6, and 12 months
Secondary Outcome Measure Information:
Title
Weight loss
Description
weight loss achieved at 3, 6 and 12 months
Time Frame
3, 6, and 12 months
Title
Clinical meaningful weight loss
Description
Percentage of participants achieving clinically significant weight loss (percentage of patients who lost >3% or >5% of their initial bodyweight)
Time Frame
3, 6, and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Overweight or obese participants who are of 19 years or older and have internet access Exclusion Criteria: Not meeting the inclusion criteria.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tzeyu Michaud, PhD
Organizational Affiliation
University of Nebraska
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nebraska Medicine Fontenelle clinic
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68104
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data obtained through this study may be provided to qualified researchers with academic interest in vaping cessation program targeting youth/young adults. Data shared will be coded, with no PHI included. Approval of the request and execution of all applicable agreements (i.e. a data transfer/use agreement) are prerequisites to the sharing of data with the requesting party.
IPD Sharing Time Frame
Data requests can be submitted starting 12 months after article publication and the data will be made accessible for up to 24 months. Extensions will be considered on a case-by-case basis
IPD Sharing Access Criteria
Access to trial IPD can be requested by qualified researchers engaging in independent scientific research, and will be provided following review and approval of a research proposal and Statistical Analysis Plan (SAP) and execution of a Data Sharing/USE Agreement.
Citations:
PubMed Identifier
32920241
Citation
Michaud TL, Estabrooks PA, You W, McGuire TJ, Almeida F, Karls K, Love K, King K, Hill J, Reed J, Porter G, Su D. Sustaining the reach of a scalable weight loss intervention through financial incentives- a pragmatic, feasibility, online randomized trial protocol. Contemp Clin Trials. 2020 Nov;98:106142. doi: 10.1016/j.cct.2020.106142. Epub 2020 Sep 10.
Results Reference
derived

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Sustaining the Reach of a Scalable Weight Loss Intervention Through Financial Incentives

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