Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
5 participants
INTERVENTIONAL
2019-03-11
2019-05-17
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Behavioral Weight Loss + Healthy Thinking
Participants 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 + Healthy Thinking
Participants will receive a 4-week behavioral weight loss intervention based on evidence-based weight loss strategies focused on diet, exercise, and behavioral skills.
Behavioral Weight Loss + Future Thinking
Participants 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.
Behavioral Weight Loss + Future Thinking
Participants will receive a 4-week behavioral weight loss intervention based on evidence-based weight loss strategies focused on diet, exercise, and behavioral skills.
Interventions
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Behavioral Weight Loss + Future Thinking
Participants will receive a 4-week behavioral weight loss intervention based on evidence-based weight loss strategies focused on diet, exercise, and behavioral skills.
Behavioral Weight Loss + Healthy Thinking
Participants will receive a 4-week behavioral weight loss intervention based on evidence-based weight loss strategies focused on diet, exercise, and behavioral skills.
Eligibility Criteria
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Inclusion Criteria
* Body Mass Index between 30-50
* English Speaking
* Have a smartphone that can be used for study activities
Exclusion Criteria
* 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.
18 Years
70 Years
ALL
No
Sponsors
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National Institute of Nursing Research (NINR)
NIH
University at Buffalo
OTHER
Kent State University
OTHER
University of Southern California
OTHER
University of Connecticut
OTHER
Responsible Party
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Amy Gorin
Principal Investigator
Locations
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UConn Weight Management Research Laboratory
Hartford, Connecticut, United States
Countries
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Other Identifiers
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H19-008
Identifier Type: -
Identifier Source: org_study_id
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