Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06744413

Prehabilitation to Improve Heart Rate Variability (PRIME)

Led by Università Vita-Salute San Raffaele · Updated on 2025-08-06

600

Participants Needed

4

Research Sites

97 weeks

Total Duration

On this page

Sponsors

U

Università Vita-Salute San Raffaele

Lead Sponsor

D

Dott. Fabio Guarracino

Collaborating Sponsor

AI-Summary

What this Trial Is About

Cancer patients require chronic management and care. For those individuals living with cancer, a comprehensive approach that acknowledges the interdisciplinary nature of their condition can help guide appropriate care strategies and support their overall well-being. Approximately 45% of patients diagnosed with cancer undergo surgery to remove their tumor. Despite the advancements in surgical techniques, anesthesia, and perioperative care, major cancer surgeries still pose a significant challenge leading to a considerable decline in physiological and functional capacity. Traditionally, efforts focused on postoperative rehabilitation to enhance recovery. Recently, prehabilitation, a form of rehabilitation which aims to improve functional capacity before surgery, has gained attention for its potential benefits in improving surgical outcomes. However, prehabilitation lacks objective assessment measures to evaluate its effectiveness. Developing validated outcome measures is essential to enhance the impact of prehabilitation on surgical outcomes and long-term care for cancer patients. Heart rate variability (HRV) is a physiological parameter that measures the variation in time intervals between consecutive heartbeats, reflecting the autonomic nervous system activity which might serve as a valuable solution for objective outcome measures in evaluating the effectiveness of prehabilitation for cancer patients, providing an objective tool to assess and monitor physiological response to stress, recovery capacity, and autonomic nervous system activity. A multicenter randomized controlled trial will be conducted to assess the impact of a multimodal prehabilitation program on HRV. Patients aged 18 or older, scheduled for elective major cancer surgery will be randomized to receive either prehabilitation or standard care. The prehabilitation arm will receive a program involving home-based physical, nutritional, and psychological interventions for at least four weeks. Participants allocated to the control group will receive usual care. Patients will be followed throughout the study using an innovative mobile application, allowing for real-time monitoring and data collection during the prehabilitation program. The study has two primary outcomes: A) to assess the impact of prehabilitation on increasing preoperative HRV in chronic cancer patients undergoing surgery; B) to assess the effect of prehabilitation on length of hospital stay.

CONDITIONS

Official Title

Prehabilitation to Improve Heart Rate Variability (PRIME)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Scheduled to undergo elective major abdominal or thoracic cancer surgery
  • Surgery planned at least three weeks after enrollment
  • Age 18 years or older
  • Provide written informed consent
  • Willing and able to use a smartphone application
Not Eligible

You will not qualify if you...

  • Very poor functional capacity
  • American Society of Anesthesiologists (ASA) physical status class 5 or 6
  • Disabling orthopedic, neuromuscular, or psychiatric diseases or other conditions preventing participation in prehabilitation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Azienda Ospedaliero Universitaria Policlinico San Marco di Catania

Catania, Italy, 95100

Active, Not Recruiting

2

Università di Foggia

Foggia, Italy, 71100

Actively Recruiting

3

IRCCS Ospedale San Raffaele

Milan, Italy, 20132

Actively Recruiting

4

Azienda Ospedaliero Universitaria Pisana

Pisa, Italy, 56126

Actively Recruiting

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Research Team

F

Fabio Guarracino, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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