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STRess Assessment of INterventional Cardiology Fellows and Attendings

STRess Assessment of INterventional Cardiology Fellows and Attendings

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07804927
Enrollment
15
Registered
2026-09-04
Start date
2023-10-04
Completion date
2027-10-04
Last updated
2026-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Brief summary

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.

Interventions

None listed

Sponsors

Minneapolis Heart Institute Foundation
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

1. Interventional Cardiology fellow or attending. 2. Age 18 years or older. 3. Willing and able to provide informed consent. 4. Access to smartphone (Apple or Android platform). 5. 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.

Design outcomes

Primary

MeasureTime frameDescription
Heart Rate Variability (HRV)From enrollment to end of study period at 14 daysHeart Rate Variability (HRV) as assessed by the wearable devices

Secondary

MeasureTime frameDescription
StressBaseline and at the end of study period at 14 daysSubjective stress assessed by the STAI-short version at baseline, before and after a procedure. Higher scores on the STAI indicate greater anxiety
Procedural characteristicsPerioperativeProcedural characteristics as assessed by the post-procedural questionnaire
BurnoutFrom enrollment to end of study period at 14 daysBurnout as assessed by the Mini-Z survey. A higher score indicates increased burnout
Heart RateFrom enrollment to end of study period at 14 daysHeart rate as assessed by the wearable device(s).
SleepFrom enrollment to end of study period at 14 daysSleep metrics as assessed by the wearable device(s).
Blood oxygenFrom enrollment to end of study period at 14 daysBlood oxygen as assessed by the wearable device(s).
Respiratory rateFrom enrollment to end of study period at 14 daysRespiratory rate as assessed by the wearable device(s).
Body temperatureFrom enrollment to end of study period at 14 daysBody temperature as assessed by the wearable device(s).
Workout metricsFrom enrollment to end of study period at 14 daysWorkout metrics as assessed by the wearable device(s).
Energy consumptionFrom enrollment to end of study period at 14 daysEnergy consumption as assessed by the wearable device(s).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026