search
Back to results

Preventing Weight Gain Among Those Who Decline Behavioral Weight Loss Treatment (STEADY) (STEADY)

Primary Purpose

Overweight and Obesity

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Steady Intervention
Sponsored by
University of Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Overweight and Obesity

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-70
  • Body weight recorded in EHR in the prior month from a primary care setting.
  • Last BMI in EHR either ≥30 kg/m2 or between 25.0-29.9 kg/m2 with documented weight-related comorbidity (hypertension, type II diabetes, pre-diabetes, dyslipidemia, sleep apnea).
  • Weight ≤ 375 lbs.
  • Self-report sending and receiving at least one text message per month for past 6 months.
  • Not currently enrolled in comprehensive behavioral weight loss treatment.
  • Respond "no" to question asking if they would like to enroll in a comprehensive weight loss program in the next month
  • Has not engaged in self-weighing ≥ 5 times per week on average over prior month.
  • Not pregnant, breastfeeding, or planning to become pregnant in next 6 months.
  • Not currently undergoing radiation or chemotherapy for cancer.
  • No history of eating disorders.
  • Interested in enrolling in low-burden self-weighing intervention.
  • Able to read and understand English without help

Exclusion criteria:

  • History of Congestive Heart Failure or heart attack in past 6 months.
  • Planning to move out of the region in the following 12 months
  • Answer incorrectly on an attention check/ validation survey item

Sites / Locations

  • UF Health at the University of FloridaRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Steady Intervention

Arm Description

Participants asked to engage in Steady Intervention for 12 months

Outcomes

Primary Outcome Measures

Intervention satisfaction
(NOTE: this is a pilot study and there is not a true primary outcome. There are several descriptive outcomes that will inform our decision to proceed to a traditional, fully powered clincial trial). Intervention satisfaction will be measured on a on 12-item study specific questionnaire asking about satisfaction with various aspects of program, such as usability, helpfulness, and if they would recommend program to a friend. This is a study specific measure without a measure name. Items will be presented separately and not combined for a total scale. Descriptive data (means, SD, range) will be presented on each item. For some items, higher numbers is better and for other items lower numbers are better.

Secondary Outcome Measures

Retention in study
Portion of participants completing 12 month survey. (There is no measurement used for this. It is based on the portion of patients who complete the 12 month survey.)
Engagement in self weighing, first quarter
Portion of participants weighing themselves on home smart scale 6 or more days per week for 9 or more weeks in first quarter of intervention. (There is no measurement used for this, it is based on the portion of participants who meet the specified threshold of self-weighing based on data obtained from the smart scale)
Engagement in self weighing, final quarter
Portion of participants weighing themselves on home smart scale 6 or more days for 9 or more weeks in final quarter of intervention. (There is no measurement used for this, it is based on the portion of participants who meet the specified threshold of self-weighing based on data obtained from the smart scale)
Portion of patients who enroll
Portion of those who are eligible who are interested in and enroll in the Steady Intervention out of those who complete the screening measure. (There is no measurement used for this, it is based on the portion of participants who enroll)
Representatives of those who enroll
Portion who enroll who are male, Black/African American, and Latino.(There is no measurement used for this, it is based on the frequency of participants who identify with these races/ethnicity)
Use of evidence-based resources offered
Portion of those offered additional resources as part of the intervention who view it and portion who initiate use of resources. (this is a behavioral outcome, based on portion who view and use resources)
Obtainment of weight data from EHR
Portion of those who enroll who have at least one weight measure in EHR between months 9-15 (there is no measure for this, it is based on portion who have a weight in their EHR)

Full Information

First Posted
February 9, 2021
Last Updated
September 15, 2022
Sponsor
University of Florida
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
search

1. Study Identification

Unique Protocol Identification Number
NCT04751656
Brief Title
Preventing Weight Gain Among Those Who Decline Behavioral Weight Loss Treatment (STEADY)
Acronym
STEADY
Official Title
Preventing Weight Gain Among Those Who Decline Behavioral Weight Loss Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 16, 2021 (Actual)
Primary Completion Date
January 31, 2023 (Anticipated)
Study Completion Date
January 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Florida
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

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
To prevent weight gain while overcoming these common barriers to engaging in weight management interventions, we propose an intervention that prescribes self-weighing but does not prescribe changes in diet or physical activity behaviors or require attendance at didactic-focused meetings. The potential of self-weighing to promote weight management is supported both by self-regulatory theory and empirical research. Promoting self-weighing may activate participants' self-regulatory skills, leading to spontaneous decisions to reduce calorie intake or increase physical activity, thus preventing further weight gain. The proposed intervention will also provide individuals with text message-based feedback to promote continued self-weighing and to motivate engagement with evidence-based resources for weight management at a time when they may be more open to using these resources-e.g., after experiencing a small weight gain. The current proposal will investigate the feasibility and acceptability of this low burden self-weighing intervention in order to prepare for a fully-powered, pragmatic randomized controlled trial. We will enroll 40 patients with either obesity or overweight with a weight-related comorbidity and who have declined to participate in a comprehensive behavioral weight management program. Participants will be asked to weigh themselves daily via a "smart" scale that transmits weight data directly to the study team via the cellular network. Every-other week, participants will be sent text messages providing brief feedback encouraging continued self-weighing. Moreover, if a small weight gain is observed, participants will be sent text messages aiming to engage them in commercial or community-based evidence-based weight management resources. In a single-arm design, all enrolled participants will receive the intervention for 12 months and will complete assessments at 3 and 12 months to assess feasibility and acceptability of the intervention and trial design, while weight will be obtained from participants' Electronic Health Records (EHR). We will evaluate our success in meeting pre-specified metrics for trial feasibility and intervention acceptability outcomes, including intervention enrollment, intervention satisfaction, and obtainment of weight data abstracted from participants' EHRs. We will also evaluate the success of the intervention in promoting regular self-weighing and use of evidence-based weight management resources.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single-arm trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Steady Intervention
Arm Type
Experimental
Arm Description
Participants asked to engage in Steady Intervention for 12 months
Intervention Type
Behavioral
Intervention Name(s)
Steady Intervention
Intervention Description
Participants will be asked to weigh themselves daily via a "smart" scale that transmits weight data directly to the study team via the cellular network for 12 months. Every-other week, participants will be sent text messages providing brief feedback encouraging continued self-weighing. Moreover, if a small weight gain is observed, participants will be sent text messages aiming to engage them in commercial or community-based evidence-based weight management resources.
Primary Outcome Measure Information:
Title
Intervention satisfaction
Description
(NOTE: this is a pilot study and there is not a true primary outcome. There are several descriptive outcomes that will inform our decision to proceed to a traditional, fully powered clincial trial). Intervention satisfaction will be measured on a on 12-item study specific questionnaire asking about satisfaction with various aspects of program, such as usability, helpfulness, and if they would recommend program to a friend. This is a study specific measure without a measure name. Items will be presented separately and not combined for a total scale. Descriptive data (means, SD, range) will be presented on each item. For some items, higher numbers is better and for other items lower numbers are better.
Time Frame
12 months.
Secondary Outcome Measure Information:
Title
Retention in study
Description
Portion of participants completing 12 month survey. (There is no measurement used for this. It is based on the portion of patients who complete the 12 month survey.)
Time Frame
12 months
Title
Engagement in self weighing, first quarter
Description
Portion of participants weighing themselves on home smart scale 6 or more days per week for 9 or more weeks in first quarter of intervention. (There is no measurement used for this, it is based on the portion of participants who meet the specified threshold of self-weighing based on data obtained from the smart scale)
Time Frame
months 0-3
Title
Engagement in self weighing, final quarter
Description
Portion of participants weighing themselves on home smart scale 6 or more days for 9 or more weeks in final quarter of intervention. (There is no measurement used for this, it is based on the portion of participants who meet the specified threshold of self-weighing based on data obtained from the smart scale)
Time Frame
months 9-12
Title
Portion of patients who enroll
Description
Portion of those who are eligible who are interested in and enroll in the Steady Intervention out of those who complete the screening measure. (There is no measurement used for this, it is based on the portion of participants who enroll)
Time Frame
at recruitment
Title
Representatives of those who enroll
Description
Portion who enroll who are male, Black/African American, and Latino.(There is no measurement used for this, it is based on the frequency of participants who identify with these races/ethnicity)
Time Frame
At recruitment
Title
Use of evidence-based resources offered
Description
Portion of those offered additional resources as part of the intervention who view it and portion who initiate use of resources. (this is a behavioral outcome, based on portion who view and use resources)
Time Frame
12 months
Title
Obtainment of weight data from EHR
Description
Portion of those who enroll who have at least one weight measure in EHR between months 9-15 (there is no measure for this, it is based on portion who have a weight in their EHR)
Time Frame
Month 15

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-70 Body weight recorded in EHR in the prior month from a primary care setting. Last BMI in EHR either ≥30 kg/m2 or between 25.0-29.9 kg/m2 with documented weight-related comorbidity (hypertension, type II diabetes, pre-diabetes, dyslipidemia, sleep apnea). Weight ≤ 375 lbs. Self-report sending and receiving at least one text message per month for past 6 months. Not currently enrolled in comprehensive behavioral weight loss treatment. Respond "no" to question asking if they would like to enroll in a comprehensive weight loss program in the next month Has not engaged in self-weighing ≥ 5 times per week on average over prior month. Not pregnant, breastfeeding, or planning to become pregnant in next 6 months. Not currently undergoing radiation or chemotherapy for cancer. No history of eating disorders. Interested in enrolling in low-burden self-weighing intervention. Able to read and understand English without help Exclusion criteria: History of Congestive Heart Failure or heart attack in past 6 months. Planning to move out of the region in the following 12 months Answer incorrectly on an attention check/ validation survey item
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Megan McVay, PhD
Phone
352-294-7029
Email
megan.mcvay@ufl.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Megan McVay, PhD
Organizational Affiliation
University of Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
UF Health at the University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Megan McVay, PhD
Phone
352-294-1638
Email
megan.mcvay@ufl.edu
First Name & Middle Initial & Last Name & Degree
Megan McVay, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The dataset will be prepared according to requirements for NHLBI data repository datasets and will be stored in the NHLBI data repository.
IPD Sharing Time Frame
Per guidelines for sharing in the NHLBI repository, the data set will be submitted to the NHLBI program officer as soon as it is prepared, and no later than 3 years after the end of clinical activities.
IPD Sharing Access Criteria
Consistent with NHLBI repository guidelines.

Learn more about this trial

Preventing Weight Gain Among Those Who Decline Behavioral Weight Loss Treatment (STEADY)

We'll reach out to this number within 24 hrs