NCT04676698

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
223

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 21, 2020

Completed
1 month until next milestone

Study Start

First participant enrolled

February 3, 2021

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 28, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 28, 2021

Completed
Last Updated

December 3, 2021

Status Verified

December 1, 2021

Enrollment Period

7 months

First QC Date

December 15, 2020

Last Update Submit

December 2, 2021

Conditions

Keywords

SatisfactionDepression

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

EXPERIMENTAL

Three times weekly for three weeks, participants will receive a text-based survey asking them to type or dictate "three good things."

Behavioral: Three Good Things

Waitlist Control Arm then Three Good Things

ACTIVE COMPARATOR

Participants will have surveys in the waiting period for 3 months and then be crossed over to the treatment arm Three Good Things.

Behavioral: Wait list control arm and then 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.

Three Good Things

Surveys will be completed for 3 months prior to treatment and then after treatment.

Waitlist Control Arm then Three Good Things

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Occupational StressPersonal SatisfactionDepression

Condition Hierarchy (Ancestors)

Occupational DiseasesStress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Katherine Gold, MD

    University of Michigan

    PRINCIPAL INVESTIGATOR

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

Locations