Surgical Prehabilitation in Abdominal Surgery (SPAS)

Universidad del Rosario

Status

Completed

Conditions

Older People

Surgical Procedure

Prehabilitation

Treatments

Behavioral: Multimodal prehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT05057741

CEI DVO005 1567-CV1324

B- 17-2020 (Other Grant/Funding Number)

Details and patient eligibility

About

Randomized clinical trial evaluating changes in functional capacity, postoperative complications and 30-day mortality in patients over 60 years of age undergoing major gastrointestinal surgery who participate in a multimodal prehabilitation program, compared to non-prehabilitated patients.

Full description

Introduction: A surgical procedure can have repercussions on the functionality and quality of life of patients, reducing their functional capacity by up to 40%; poor preoperative physical performance increases the risk of perioperative morbidity and mortality by 30% and prolongs functional recovery, increasing the hospital stay of the older adult. Prehabilitation is a preoperative intervention that improves the physical, psychological and nutritional condition of the patient to obtain a better postoperative recovery, mobility and functional independence.

Objective: To evaluate changes in functional capacity, postoperative complications and 30-day mortality in patients over 60 years of age undergoing major gastrointestinal surgery who participate in a multimodal prehabilitation program (exercise, nutrition and relaxation).

Methodology: Randomized clinical trial. Two study groups will be compared, an experimental group that will receive the educational intervention (multimodal prehabilitation program) and a control group that will continue with the usual management in the Hospital. The project activities will be carried out in Telehealth modality due to COVID-19 contagion containment measures.

Expected results: To encourage interprofessional work based on common goals with standardization of data and processes to improve physical condition and reduce post-surgical complications; to establish traceability of care, clinical and functional condition of the patient. It is intended to generate scientific evidence, integrate the research groups Méderi, Rehabilitation Sciences and Clinical Research.

Enrollment

24 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients scheduled by the General Surgery, Coloproctology and Hepatobiliary Surgery services
Cognitive ability to follow instructions,
Understand the material delivered (basic reading comprehension - through physical or digital media)
Perform physical exercise.
Aptitude to exercise according to the cardiovascular risk assessment performed by the treating physician.

Exclusion criteria

Patients scheduled for surgery from the emergency department
Patients with sepsis,
Patients with metastatic disease, without curative perspective
Patients with dysphagia for solid foods
Patients with incapacitating psychiatric or neurological illnesses
Patients with documented previous immunosuppression status (corticosteroid users in the 6 weeks prior to the randomisation) and/or HIV
Diabetic patients, with chronic renal disease, stage 4-5, with renal replacement therapy
Patients with heart failure decompensated, or that limits the physical exercise
Patients with dependent mobility
Patients with history of second primary neoplasm