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Protocol for Prehabilitation Service Implementation in Catalonia

Protocol for Prehabilitation Service Implementation in Catalonia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03767387
Enrollment
750
Registered
2018-12-06
Start date
2018-11-01
Completion date
2019-10-01
Last updated
2020-02-13

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

Conditions

Chronic Disease

Keywords

Prehabilitation, Physical Activity, Integrated Care, Collaborative Self-management

Brief summary

Trimodal prehabilitation consists of a short-term (\ four to six weeks) preventive intervention to: i) enhance aerobic capacity and daily physical activity; ii) nutritional optimization; and, iii) psychological support before a major surgical procedure. The final aim of prehabilitation is to decrease surgical complications and speed-up postoperative functional recovery.

Detailed description

This is a preventive intervention addressed to high risk candidates for major surgical procedures carried out for a period of approximately four weeks before surgery aiming at reducing complications and enhancing post-surgical recovery. It combines: i) high-intensity endurance exercise training and promotion of daily physical activity; ii) nutritional balance; and, iii) psychological support. The intervention is currently deployed as mainstream service at Hospital Clinic in several types of major surgeries. During fall 2017, three multidisciplinary workshops using a design-thinking approach were carried out to refine the service workflow and to explore the potential for service scalability. The outcomes of the co-design process provided a robust background for the design of a future personalized perioperative care service at regional level covering three phases: prehabilitation, in-patient care, and, post-discharge care. The current study protocol aims to assess cost-effectiveness of prehabilitation as mainstream service in the ongoing deployment at Hospital Clinic, as well as to generate a roadmap for regional scalability of the service. It is planned as a quasi-experimental case-control study including 500 patients undertaking prehabilitation, as intervention group, and 250 patients following standard conventional care before surgery. The patients will be included from the following type of surgeries (2:1 intervention to control ratio): major digestive surgery (n, 525), lung volume reduction (n, 30), radical cystectomy (n, 30), major cardiovascular surgery (n, 165). Study groups will be made comparable using propensity score matching with the following matching variables: type of surgery, age, sex and adjusted morbidity groups (GMA) scoring.

Interventions

Prehabilitation before major surgery consisting of: i) motivational interview to assess patient's adherence profile and to co-design the characteristics of the physical activity program with the patient; ii) personalised program to promote daily physical activity; and iii) supervised high-intensity endurance exercise training program.

Sponsors

Hospital Clinic of Barcelona
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* Adult patients (\>18 years old) candidates to colorectal surgery, esophagectomy, gastrectomy, gastric bypass, major liver resection, pancreas resection, lung volume resection, radical cystectomy, cardiac valve surgery or cardiac revascularization. * Patients at high-risk for surgical complications defined by age \> 70 years old and/or American Society of Anesthesiologists 3-4.

Exclusion criteria

* Non-elective surgery * Metastatic disease known preoperatively * Unstable cardiac or respiratory disease * Locomotor limitations precluding exercise performance * Cognitive deterioration impeding adherence to the program

Design outcomes

Primary

MeasureTime frameDescription
cost-effectiveness4 weeksHealth care costs

Secondary

MeasureTime frameDescription
Number of hospital readmissions4 weeks30-day hospital readmissions rate
Number of Emergency room visits4 weeks30-day emergency room visits rate
Meters achieved in the six-minute walk test4 weeksAerobic capacity
Length of stay4 weekshospital and intensive care unit length of stay,
Complications4 weeksnumber of complications per patient
Health status assessed by 36-Item Short Form Survey (SF-36)4 weeksHealth status related quality of life (Range 0-100) Higher values represent better
Psychological status assessed by the The Hospital Anxiety And Depression Scale (HAD)4 weeksPsychological status (Range 0-21) Higher values represent worst
Yale Physical Activity Survey (YPAS)4 weeksPhysical activity assessed by the YPAS (Range 0-100) Higher values represent better

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026