The Gratitude Gallery - A Positive Psychology Intervention
NCT ID: NCT04723251
Last Updated: 2021-12-17
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
13 participants
INTERVENTIONAL
2021-03-16
2021-11-02
Brief Summary
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The study hypothesizes that participants will find the activity feasible and acceptable and complete the intervention as directed. The project also hypothesizes that those that complete the intervention will show an increase in self-reported gratitude, as well as a decrease in symptoms of anxiety and depression.
Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Taking Photographs
Participants will be asked to take photos with their cell phone.
taking photographs
Participants will photograph images (using a cell phone) that invoke a feeling of gratitude. At least 1 photograph (at any time of the day) should be taken for a period of three weeks.
Once the photo images are captured, the participant should spend a moment looking at the image and reflecting on why they are grateful for the subject of the photograph.
Interventions
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taking photographs
Participants will photograph images (using a cell phone) that invoke a feeling of gratitude. At least 1 photograph (at any time of the day) should be taken for a period of three weeks.
Once the photo images are captured, the participant should spend a moment looking at the image and reflecting on why they are grateful for the subject of the photograph.
Eligibility Criteria
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Inclusion Criteria
* Owns a smart phone capable of taking pictures
* Willing and able to comply with all aspects of study procedures
* PHQ-9 score greater or equal to 5 but less or equal to 14 with no suicidal ideation
* Generalized anxiety disorder (GAD-7) score greater or equal to 0 but less or equal to 9
* No plan to initiate a new program that could increase positive affect during the study period (e.g., psychotherapy, new exercise regimen, meditation classes)
* If on medication then stable (at least 3 months) on dose or not on medication
Exclusion Criteria
* Other factors that at the discretion of the investigators that would adversely affect study participation
18 Years
65 Years
ALL
No
Sponsors
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University of Michigan
OTHER
Responsible Party
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Erin Hendriks
Assistant Professor of Family Medicine
Principal Investigators
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Erin Hendriks, MD
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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University of Michigan
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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HUM00177310
Identifier Type: -
Identifier Source: org_study_id