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STRess Assessment of INterventional Cardiology Fellows and Attendings

31 augusti 2026 uppdaterad av: 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.

Studieöversikt

Status

Rekrytering

Betingelser

Påfrestning

Studietyp

Observationell

Inskrivning (Beräknad)

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

Förenta staterna
- Minnesota
  - Minneapolis, Minnesota, Förenta staterna, 55407
    - Rekrytering
    - Minneapolis Heart Institute Foundation
    - Kontakt:
      
      Bavana V Rangan, BDS, MPH
      
      Telefonnummer: 817-821-9945
      
      E-post: bavana.rangan@allina.com

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

Vuxen
Äldre vuxen

Tar emot friska volontärer

N/A

Testmetod

Icke-sannolikhetsprov

Studera befolkning

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

Beskrivning

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

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Vad mäter studien?

Primära resultatmått

Resultatmått	Åtgärdsbeskrivning	Tidsram
Heart Rate Variability (HRV) Tidsram: 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

Sekundära resultatmått

Resultatmått	Åtgärdsbeskrivning	Tidsram
Stress Tidsram: 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 Tidsram: Perioperative	Procedural characteristics as assessed by the post-procedural questionnaire	Perioperative
Burnout Tidsram: 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 Tidsram: 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 Tidsram: 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 Tidsram: 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 Tidsram: 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 Tidsram: 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 Tidsram: 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 Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Minneapolis Heart Institute Foundation

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

4 oktober 2023

Primärt slutförande (Beräknad)

4 oktober 2027

Avslutad studie (Beräknad)

4 oktober 2027

Studieregistreringsdatum

Först inskickad

17 augusti 2026

Först inskickad som uppfyllde QC-kriterierna

31 augusti 2026

Första postat (Faktisk)

4 september 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)