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NCT Number: NCT07804927

STRess Assessment of INterventional Cardiology Fellows and Attendings

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Minneapolis Heart Institute Foundation

Minneapolis, Minnesota, 55407, United States

Location status: Recruiting

Location contact

Bavana V Rangan, BDS, MPH

CONTACT

[email protected]

817-821-9945

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Heart Rate Variability (HRV)

    Time frame: From enrollment to end of study period at 14 days

    Heart Rate Variability (HRV) as assessed by the wearable devices

Secondary outcomes

  1. Stress

    Time frame: 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

  2. Procedural characteristics

    Time frame: Perioperative

    Procedural characteristics as assessed by the post-procedural questionnaire

  3. Burnout

    Time frame: From enrollment to end of study period at 14 days

    Burnout as assessed by the Mini-Z survey. A higher score indicates increased burnout

  4. Heart Rate

    Time frame: From enrollment to end of study period at 14 days

    Heart rate as assessed by the wearable device(s).

  5. Sleep

    Time frame: From enrollment to end of study period at 14 days

    Sleep metrics as assessed by the wearable device(s).

  6. Blood oxygen

    Time frame: From enrollment to end of study period at 14 days

    Blood oxygen as assessed by the wearable device(s).

  7. Respiratory rate

    Time frame: From enrollment to end of study period at 14 days

    Respiratory rate as assessed by the wearable device(s).

  8. Body temperature

    Time frame: From enrollment to end of study period at 14 days

    Body temperature as assessed by the wearable device(s).

  9. Workout metrics

    Time frame: From enrollment to end of study period at 14 days

    Workout metrics as assessed by the wearable device(s).

  10. Energy consumption

    Time frame: From enrollment to end of study period at 14 days

    Energy consumption as assessed by the wearable device(s).

Sponsors and collaborators

Lead sponsor

Minneapolis Heart Institute Foundation

Other

Registry information

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Sep 4, 2026
Registry last updated
Sep 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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