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
60 participants
INTERVENTIONAL
2013-12-12
2017-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
DIAGNOSTIC
SINGLE
Study Groups
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Stress Condition
The stress condition involved the Trier Social Stress Test (TSST), a standardized laboratory stressor designed to elicit psychological stress and cortisol responses. Following the TSST, participants were brought to a separate room, instructed to rest and given the option to eat at their leisure. Books and magazines were included in the room for the participant to utilize.
Acute Laboratory Stressor
The TSST was 20 minutes long and consisted of a five-minute instructional period where participants listened to a pre-recorded tape; a five-minute speech preparation period; a five-minute challenging serial subtraction task; and a five-minute videotaped public speaking task in front of a panel of three evaluative, non-affirming judges dressed in white coats.
Rest Condition
Participants completed a control condition on a separate day. This condition followed the same sequence of events as the stress condition with the exception that the 20-minute TSST was replaced with a 20-minute low-affect educational film screening.
Low affect video
The 20-minute TSST was replaced with a 20-minute low-affect educational film screening.
Interventions
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Acute Laboratory Stressor
The TSST was 20 minutes long and consisted of a five-minute instructional period where participants listened to a pre-recorded tape; a five-minute speech preparation period; a five-minute challenging serial subtraction task; and a five-minute videotaped public speaking task in front of a panel of three evaluative, non-affirming judges dressed in white coats.
Low affect video
The 20-minute TSST was replaced with a 20-minute low-affect educational film screening.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Had been enrolled in a weight loss program in the last 6 months
* Were current smokers (e.g., tobacco, marijuana, vaping)
* Were diagnosed with a mental health condition (e.g, depression)
* Were diagnosed with a chronic condition known to affect weight, appetite, blood glucose or insulin levels (e.g., diabetes)
* Were taking medications known to affect metabolic processes (e.g., growth hormone, ritalin, metformin, etc)
* Had food allergies, intolerances, or other dietary restrictions
14 Years
19 Years
ALL
Yes
Sponsors
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University of Michigan
OTHER
Responsible Party
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Rebecca Hasson
Director, Childhood Disparities Research Laboratory
Principal Investigators
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Rebecca Hasson, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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Childhood Disparities Research Laboratory
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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HUM00078153
Identifier Type: -
Identifier Source: org_study_id
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