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Trimodal Prehabilitation in Patients Undergoing Elective Surgery

The Influence of Prehabilitation on the Surgical Patients Condition

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05114408
Enrollment
40
Registered
2021-11-10
Start date
2012-06-07
Completion date
2021-12-31
Last updated
2021-11-10

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

Conditions

Cardiac Complication, Perioperative Complication

Brief summary

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

Detailed 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.

Interventions

OTHER4 week trimodal prehabilitation course

trimodal prehabilitation in mixed: stationary and at-home structure

Sponsors

University Clinical Centre, Gdansk
CollaboratorOTHER
EIT Health
CollaboratorOTHER
Medical University of Gdansk
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Perceives stress - Perceived Stress Questionaire (PSS)baseline and pre surgerystress level - 0 - min value - no perceived stress 20 - maximal preceived stress
Global Leadership Initiative on Malnutrition (GLIM) scalebaseline and pre surgerychange in nutritional status - malnutrition diagnosed if one phenotypical and one etiological criteria are fulfilled Severity based on phenotypic criteria: 1. minimal value (moderate malnutrition) 2. max value (severe malnutrition)
6 minute walk testbaseline and pre surgerychange in aerobic capacity
Yale Physical Activity Survey (YPAS)baseline and pre surgerychange in physical activity
self-perceived health status scale (36-Item Short Form Survey - SF36)baseline and pre surgerychange in self-perceived health status (0 - min, 100 - max self perceived health score)
motivation questionaire (MQ)baseline and pre surgerychange in patient's motivation 0-10 0 - low motiwation 10 max motivation
Hospital Anxiety and Depression (HAD) scalebaseline and pre surgerychange in psychological status: depression and anxiety criteria 0 points min score - low level od depression and anxiety 21 max score

Secondary

MeasureTime frameDescription
Number of Patients with postoperative complications3 month after surgerynumber and severity
Number of Participants requiring reintervention during initial hospitalization3 months after surgery
ICU length of stay3 months after surgery
Total hospital length of stay3 months after surgery
Number of Patients requiring Emergency room visits and hospital readmissionsat 30 days

Other

MeasureTime frameDescription
Patient concentration questionaire (P3CQ)after prehabilitation coursePatient experience: 0 - worst (medical staff not concentrated on patient) 19 - best experience (full concentration on patients needs)
Continuity of Care Questionaire (NCQ)after prehabilitation courseform 0 - 5 pints 0 - lack of continuity of care 5 - maximal continuitu of care
cost analysis3 months after surgery
Staff engagement questionaire (ACT)after recruitmentStaff engagement

Countries

Poland

Contacts

Primary ContactTomasz Jasiński, MD PhD
tjasinski@uck.gda.pl+48583493280
Backup ContactMateusz Kreczko, MD
+48583493280

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026