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Physical Activity Choices Everyday- A Pilot Study

Not Applicable
Completed
Conditions
Obesity
Interventions
Behavioral: Behavioral Weight Loss + Healthy Thinking
Behavioral: Behavioral Weight Loss + Future Thinking
Registration Number
NCT03843099
Lead Sponsor
University of Connecticut
Brief Summary

This study aims to test two strategies for weight loss. Participants will be randomly assigned to one of the two 4-week weight loss programs: (1) a behavioral weight loss program that involves recording weekly weight, physical activity, and caloric intake plus daily exercises in which information about a healthy lifestyle is reviewed or (2) a behavioral weight loss program that involves recording weekly weight, physical activity, and caloric intake plus daily exercises in which descriptions of positive future events are reviewed. Throughout the study, participants will complete assessments that examine the effects of the interventions on delay discounting, physical activity, weight, and other important health and psychosocial outcomes.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
5
Inclusion Criteria
  • Age between 18-70
  • Body Mass Index between 30-50
  • English Speaking
  • Have a smartphone that can be used for study activities
Exclusion Criteria
  • Report being unable to walk 2 blocks without stopping
  • Are currently participating in weight loss treatment, have a history of bariatric surgery, or lost ≥5% in the past 6-months
  • Are pregnant or plan to become pregnant within 2 months
  • Report a heart condition, chest pain during periods of rest or activity, or loss of consciousness on the Physical Activity Readiness Questionnaire
  • Report a medical condition that could jeopardize their safety in a weight control program with diet and exercise guidelines
  • History of or current traumatic brain injury, dementia or Alzheimer's disease; a history of Multiple Sclerosis, or other neurological disorders
  • Report conditions that, in the judgment of the PI, would render them unlikely to follow the protocol (e.g., relocation, dementia, unable to read and write in English)
  • Have no Internet access or unwilling to use personal smartphone for study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Behavioral Weight Loss + Healthy ThinkingBehavioral Weight Loss + Healthy ThinkingParticipants will receive a 4-week behavioral weight loss intervention based on evidence-based weight loss strategies focused on diet, exercise, and behavioral skills. In this treatment, participants will be asked to read short passages related to nutrition and a healthy lifestyle through our study website twice a day for the duration of treatment.
Behavioral Weight Loss + Future ThinkingBehavioral Weight Loss + Future ThinkingParticipants will receive a 4-week behavioral weight loss intervention based on evidence-based weight loss strategies focused on diet, exercise, and behavioral skills. In this treatment, participants will create descriptions of upcoming positive events and will be asked to read short passages through our study website at least twice a day for the duration of treatment.
Primary Outcome Measures
NameTimeMethod
Physical Activitybaseline and week 7

Change in minutes of moderate to vigorous physical activity measured via a waist worn accelerometer during 7 day time periods.

Delay Discountingbaseline and week 7

Change in delay discounting measured using a choice task.

Secondary Outcome Measures
NameTimeMethod
Weight4 weeks

Weight change from baseline to post treatment

Trial Locations

Locations (1)

UConn Weight Management Research Laboratory

🇺🇸

Hartford, Connecticut, United States

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