ClinicalTrials.Veeva

Menu

Prehabilitation in Patients on a Waiting List for a Transplant

U

University of Malaga

Status

Withdrawn

Conditions

Transplant Dysfunction

Treatments

Device: Prehabilitation program

Study type

Interventional

Funder types

Other

Identifiers

NCT03314376
PREHAB-T

Details and patient eligibility

About

The aim of this study is to prove the effects of a individualized prehabilitation program (muscular strength and endurance) in patients in a waiting list for a transplant. The investigators want to see if patients that did a prehabilitation program have better results in the postoperative period.

Full description

Some characteristics of the fragile people, like as sarcopenia, are related with worse results after a transplant. Increasing the cardiorespiratory fitness with an exercise program during the preoperative period has shown improvements in patients after a surgery. It is produced a decreased in his functions, including a loss of muscle mass.

Prehabilitation is a exercise program before a surgery. This program will improve the patient's starting functional status and therefore recovery.

Physical activity is one of the most powerful predictors of mortality risk. Several studies say that a improved cardiorespiratory fitness by exercise before a surgery has a great impact in the patients after the intervention in short and long term.

Sex

All

Ages

50 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients on a waiting list for a transplant.
  • Fried Fragility Index >3
  • Space more than 6 week between the beginning of the exercise program and the surgery.

Exclusion criteria

  • Severe cardiovascular disease.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Prehabilitation program
Experimental group
Description:
Individualized physiotherapy strength and muscular endurance with aerobic training, led by physiotherapists in groups of 8-10 participants.
Treatment:
Device: Prehabilitation program
Control group
No Intervention group
Description:
They will be instructed to continue their current activities and not to increase objectively levels of physical activity performed during the 6-week intervention.

Trial contacts and locations

1

Loading...

Central trial contact

Antonio I Cuesta-Vargas, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems