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Three Good Things 2020: a Brief Text-based Wellness Intervention

2. december 2021 opdateret af: Katherine Gold, University of Michigan

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.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

223

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Forenede Stater
    • Michigan
      • Ann Arbor, Michigan, Forenede Stater, 48109
        • University of Michigan

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Faculty, resident, or staff in the Michigan Medicine (MM) Department of Family Medicine

Exclusion Criteria:

  • Not a member of Family Medicine at MM

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Sundhedstjenesteforskning
  • Tildeling: Randomiseret
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Three Good Things
Three times weekly for three weeks, participants will receive a text-based survey asking them to type or dictate "three good things."
Adfærdsmæssigt: Three Good Things
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.
Aktiv komparator: Waitlist Control Arm then Three Good Things
Participants will have surveys in the waiting period for 3 months and then be crossed over to the treatment arm Three Good Things.
Adfærdsmæssigt: Wait list control arm and then Three Good Things
Surveys will be completed for 3 months prior to treatment and then after treatment.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in the Positive and Negative Affect Schedule (PANAS-SF) between the intervention and control group
Tidsramme: Pre-Treatment (baseline), up to 6 months
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

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in self-reported physical health
Tidsramme: Pre-Treatment (baseline), up to 6 months
This is a 1 question item to assess participants physical health ( 1=Excellent 2=good 3=fair 4=poor).
Pre-Treatment (baseline), up to 6 months
Change in self-reported mental health
Tidsramme: Pre-Treatment (baseline), up to 6 months
This is a 1 question item to assess participants mental health ( 1=Excellent 2=good 3=fair 4=poor).
Pre-Treatment (baseline), up to 6 months
Change in Gratitude using the Gratitude Adjective Checklist (GAC)
Tidsramme: Pre-Treatment (baseline), up to 6 months
The GAC is a 3-item self-report measure of state gratitude in which participants select, (1) A little (2) Moderately, Quite a bit (4), and Extremely (5).The total score on GAC ranges from 3 to 15, with higher score indicating greater state gratitude.
Pre-Treatment (baseline), up to 6 months
Change in depression using the Patient Health Questionnaire 9-item (PHQ-9) score
Tidsramme: Pre-Treatment (baseline) to 6 months
PHQ-9 scores reflect depression severity. Participants will select responses that include 0=not at all, 1=several days, 2=more than half the days, 3=nearly every day. Ranges in scores are from 0-27 (Scores: 0-4 none, 5-9 mild, 10-14 moderate, 15-19 moderately severe, 20-27 severe).
Pre-Treatment (baseline) to 6 months
Change in Satisfaction with Life Questionnaire
Tidsramme: Pre-Treatment (baseline), up to 6 months
This is a 5 question questionnaire in which participants select from 7 responses that are given a 1-7 scale from strongly disagree to strongly agree. Scoring ranges from 5-35 where 20 = neutral (the higher the score the more satisfaction).
Pre-Treatment (baseline), up to 6 months
Change in the Hope Scale
Tidsramme: Pre-Treatment (baseline), up to 6 months

This is a 12 item questionnaire in which participants select from answers that include 1=definitely false 2=mostly false 3=mostly true 4=definitely true.

Scores range from 12-48 with higher scores indicating greater hope.
Pre-Treatment (baseline), up to 6 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

University of Michigan

Efterforskere

  • Ledende efterforsker: Katherine Gold, MD, University of Michigan

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

3. februar 2021

Primær færdiggørelse (Faktiske)

28. august 2021

Studieafslutning (Faktiske)

28. august 2021

Datoer for studieregistrering

Først indsendt

15. december 2020

Først indsendt, der opfyldte QC-kriterier

15. december 2020

Først opslået (Faktiske)

21. december 2020

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

3. december 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. december 2021

Sidst verificeret

1. december 2021

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • HUM00188399

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Jobrelateret stress

Kliniske forsøg med Three Good Things

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Sponsorer og samarbejdspartnere

Medicinske tilstande

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Betingelser

Sjældne sygdomme

Narkotikainterventioner

Kosttilskud

Sponsor / samarbejdspartnere

Placeringer

Abonner