©2022 Stanford Medicine
Ignite Pilot: Goal Setting in a Digital Weight Loss Intervention
Not Recruiting
Trial ID: NCT05715242
Purpose
The goal of this pilot trial is to learn about the optimal intensity level of goals in a
digital weight loss intervention among adults with overweight or obesity. The main questions
of the study are to assess the feasibility and acceptability of different goal intensities
across four domains (calorie goal, step goal, eating window goal, red zone food goal).
The investigators will recruit 32 total participants to the trial. Recruitment will occur
through remote channels. Interested individuals will be directed to an online screening
questionnaire; those who are eligible will then be invited to attend an initial remote
session with study personnel to ensure interest and eligibility in the study. The weight loss
intervention will last 10 weeks, and all participants will receive a "core" treatment
consisting of self-monitoring weight, food intake, and steps (all via digital tools provided
by the study team), along with behavioral lessons, action plans, and tailored feedback.
Depending on which group participants are assigned to in the study, individuals will receive
either a more or less challenging goal across the four domains. All study tasks will occur
remotely, thus, participants will never come in-person for any tasks. Assessment of body
weight and other measures will occur at the beginning of the trial ("baseline"), and at 4
weeks and 10 weeks.
The investigators will use the Multiphase Optimization Strategy (MOST) framework to identify
which of the goal intensity levels result in meaningful engagement and weight loss. The
current study is the first step towards answering this question; it is designed as a pilot
factorial trial, which focuses on feasibility and acceptability. In total, there will be 16
treatment conditions.
Official Title
Goal Setting in a Standalone, Digital Weight Loss Intervention: a Pilot Factorial Trial
Stanford Investigator(s)
Eligibility
Inclusion Criteria:
- adults (ages 18+ years)
- body mass index (BMI) 25.0 to 45.0 kg/m^2
- smartphone ownership
- willingness to install the Fitbit mobile app on their phone
- access to a personal email account
- English language proficiency
- interest in losing weight through behavioral strategies
- living in the United States
Exclusion Criteria:
- concurrent enrollment in another weight management intervention
- loss of ≥10 lbs. in the past 6 months
- current use of a weight loss medication
- prior or planned bariatric surgery
- current or planned pregnancy in the trial period
- currently breastfeeding
- lives with someone else participating in the study
- hospitalization for a mental health condition in the past 12 months
- inability to engage in moderate forms of physical activity akin to brisk walking
(assessed by the Physical Activity Readiness Questionnaire)
- if weight loss is contraindicated or might be impacted by a condition or medication
(e.g., end stage renal disease, cancer, schizophrenia, dementia, steroids,
anti-psychotics)
- if an individual would be better suited for a more intensive or different type of
intervention based on a health condition (e.g., individuals with history of an eating
disorder or cardiovascular event, uncontrolled hypertension, or uncontrolled diabetes
mellitus)
- investigator discretion for safety reasons
Intervention(s):
behavioral: Core Behavioral Weight Loss Intervention
behavioral: Easier Step Goal
behavioral: Harder Step Goal
behavioral: Easier Calorie Goal
behavioral: Harder Calorie Goal
behavioral: Easier Eating Window Goal
behavioral: Harder Eating Window Goal
behavioral: Easier Red Zone Food Goal
behavioral: Harder Red Zone Food Goal
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Michele L Patel, PhD
650-549-7047