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STRess Assessment of INterventional Cardiology Fellows and Attendings

31. august 2026 opdateret af: Minneapolis Heart Institute Foundation

Interventional cardiology (IC) fellows and attendings experience high levels of stress. In a recent study, IC fellowship was considered very stressful by 22%, somewhat stressful by 62%, and not stressful by 16%(1). In a different study, 29% of the IC fellows considered leaving their job during the past year, while more than a quarter (29%) felt overwhelmed ≥3x/week(2). Moreover, the same study reports that burnout affects 69% of the interventional cardiologists. In addition, in the Medscape Cardiologist Lifestyle, Happiness & Burnout Report 2023, 43% of the cardiologists in general reported being burned out and 23% were depressed(3). However, it remains unknown whether they deal with increased stress before, during, and after a procedure, if their stress decreases (and if so, how much) with experience, and how they recover after a procedure. The present study will study the stress levels of IC fellows and attendings using various subjective metrics and wearable devices.

Studieoversigt

Status

Rekruttering

Betingelser

Stress

Undersøgelsestype

Observationel

Tilmelding (Anslået)

Kontakter og lokationer

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

Studiesteder

Forenede Stater
- Minnesota
  - Minneapolis, Minnesota, Forenede Stater, 55407
    - Rekruttering
    - Minneapolis Heart Institute Foundation
    - Kontakt:
      
      Bavana V Rangan, BDS, MPH
      
      Telefonnummer: 817-821-9945
      
      E-mail: bavana.rangan@allina.com

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

Voksen
Ældre voksen

Tager imod sunde frivillige

N/A

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

The target study population is all interventional cardiology attendings and fellows at Minneapolis Heart Institute.

Beskrivelse

Inclusion Criteria:

Interventional Cardiology fellow or attending.
Age 18 years or older.
Willing and able to provide informed consent.
Access to smartphone (Apple or Android platform).
Willing and able to wear the wearable devices.

Exclusion Criteria:

1- Any health condition that in the opinion of the investigator would preclude individual's participation in the study such as conditions that would preclude them from wearing the study wearables and participating to provide wearable data.

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål	Foranstaltningsbeskrivelse	Tidsramme
Heart Rate Variability (HRV) Tidsramme: From enrollment to end of study period at 14 days	Heart Rate Variability (HRV) as assessed by the wearable devices	From enrollment to end of study period at 14 days

Sekundære resultatmål

Resultatmål	Foranstaltningsbeskrivelse	Tidsramme
Stress Tidsramme: Baseline and at the end of study period at 14 days	Subjective stress assessed by the STAI-short version at baseline, before and after a procedure. Higher scores on the STAI indicate greater anxiety	Baseline and at the end of study period at 14 days
Procedural characteristics Tidsramme: Perioperative	Procedural characteristics as assessed by the post-procedural questionnaire	Perioperative
Burnout Tidsramme: From enrollment to end of study period at 14 days	Burnout as assessed by the Mini-Z survey. A higher score indicates increased burnout	From enrollment to end of study period at 14 days
Heart Rate Tidsramme: From enrollment to end of study period at 14 days	Heart rate as assessed by the wearable device(s).	From enrollment to end of study period at 14 days
Sleep Tidsramme: From enrollment to end of study period at 14 days	Sleep metrics as assessed by the wearable device(s).	From enrollment to end of study period at 14 days
Blood oxygen Tidsramme: From enrollment to end of study period at 14 days	Blood oxygen as assessed by the wearable device(s).	From enrollment to end of study period at 14 days
Respiratory rate Tidsramme: From enrollment to end of study period at 14 days	Respiratory rate as assessed by the wearable device(s).	From enrollment to end of study period at 14 days
Body temperature Tidsramme: From enrollment to end of study period at 14 days	Body temperature as assessed by the wearable device(s).	From enrollment to end of study period at 14 days
Workout metrics Tidsramme: From enrollment to end of study period at 14 days	Workout metrics as assessed by the wearable device(s).	From enrollment to end of study period at 14 days
Energy consumption Tidsramme: From enrollment to end of study period at 14 days	Energy consumption as assessed by the wearable device(s).	From enrollment to end of study period at 14 days

Samarbejdspartnere og efterforskere

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

Sponsor

Minneapolis Heart Institute Foundation

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)

4. oktober 2023

Primær færdiggørelse (Anslået)

4. oktober 2027

Studieafslutning (Anslået)

4. oktober 2027

Datoer for studieregistrering

Først indsendt

17. august 2026

Først indsendt, der opfyldte QC-kriterier

31. august 2026

Først opslået (Faktiske)

4. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)