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Trimodal Prehabilitation in Patients Undergoing Elective Surgery

M

Medical University of Gdansk

Status

Unknown

Conditions

Perioperative Complication
Cardiac Complication

Treatments

Other: 4 week trimodal prehabilitation course

Study type

Interventional

Funder types

Other

Identifiers

NCT05114408
PREHAB1

Details and patient eligibility

About

Patients scheduled for elective surgery will undergo 4 week course of trimodal prehabilitation

Full description

Patients with high surgical risk will participate in 4 week prehabilitation that will consist of 4 stationary sessions - one per week - comprised of: physiotherapy session, psychological session and nutritional advice. During first session each patient will receive an activity monitor and dedicated mobile app that will record his daily performance.

Enrollment

40 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 70 and/or American Society of American Society of Anesthesiologists Physical Status Classification System (ASA) 3-4
  • Unfit patients

Exclusion criteria

  • physical condition that makes the patient is not able to perform rehabilitation exercises
  • cardiac and respiratory instability or high risk of its occurrence
  • inability to use electronic devices used in the study

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Trimodal prehabilitation
Experimental group
Description:
Patients qualified for elective surgery that meet criteria for prehabilitation
Treatment:
Other: 4 week trimodal prehabilitation course

Trial contacts and locations

1

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Central trial contact

Tomasz Jasiński, MD PhD; Mateusz Kreczko, MD

Data sourced from clinicaltrials.gov

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