Three Good Things 2020: a Brief Text-based Wellness Intervention
1 other identifier
interventional
223
1 country
1
Brief Summary
This trial will be open to all Michigan Medicine Department of Family Medicine faculty, resident, or staff. The intervention will consist of asking participants the "3 Good Things" based on positive psychology theory. Participants will be asked to list three things that went well that day and to consider their role in these outcomes. Pre and post surveys will be completed to evaluate this intervention. At the end of the trial the study team will also select a limited number of entries from participants to share some of the "good things" which people listed. These will be edited to ensure writer anonymity and participants will be informed of this plan in the study introduction.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 15, 2020
CompletedFirst Posted
Study publicly available on registry
December 21, 2020
CompletedStudy Start
First participant enrolled
February 3, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 28, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
August 28, 2021
CompletedDecember 3, 2021
December 1, 2021
7 months
December 15, 2020
December 2, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in the Positive and Negative Affect Schedule (PANAS-SF) between the intervention and control group
This is a 10 item survey to measure positive and negative affect. Responses include; very slightly or not at all, a little, quite a bit, and extremely. Higher scores of Positive Affect (PA) subscale represent higher positive affect higher scores of Negative affect (NA) subscale represent higher negative affect.
Pre-Treatment (baseline), up to 6 months
Secondary Outcomes (6)
Change in self-reported physical health
Pre-Treatment (baseline), up to 6 months
Change in self-reported mental health
Pre-Treatment (baseline), up to 6 months
Change in Gratitude using the Gratitude Adjective Checklist (GAC)
Pre-Treatment (baseline), up to 6 months
Change in depression using the Patient Health Questionnaire 9-item (PHQ-9) score
Pre-Treatment (baseline) to 6 months
Change in Satisfaction with Life Questionnaire
Pre-Treatment (baseline), up to 6 months
- +1 more secondary outcomes
Study Arms (2)
Three Good Things
EXPERIMENTALThree times weekly for three weeks, participants will receive a text-based survey asking them to type or dictate "three good things."
Waitlist Control Arm then Three Good Things
ACTIVE COMPARATORParticipants will have surveys in the waiting period for 3 months and then be crossed over to the treatment arm Three Good Things.
Interventions
The treatment phase will last 3 weeks. However, participants will complete surveys at baseline and up to 6 months. At the end of the trial the study team will also select a limited number of entries from participants to share some of the "good things" which people listed. These will be edited to ensure writer anonymity and participants will be informed of this plan in the study introduction.
Surveys will be completed for 3 months prior to treatment and then after treatment.
Eligibility Criteria
You may qualify if:
- Faculty, resident, or staff in the Michigan Medicine (MM) Department of Family Medicine
You may not qualify if:
- Not a member of Family Medicine at MM
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Michigan
Ann Arbor, Michigan, 48109, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Katherine Gold, MD
University of Michigan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of Family Medicine and Associate Professor of Obstetrics and Gynecology
Study Record Dates
First Submitted
December 15, 2020
First Posted
December 21, 2020
Study Start
February 3, 2021
Primary Completion
August 28, 2021
Study Completion
August 28, 2021
Last Updated
December 3, 2021
Record last verified: 2021-12
Data Sharing
- IPD Sharing
- Will not share