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Clinical Trials/NCT04892368
NCT04892368
Unknown
N/A

Prospective Single-centre Randomized Controlled Trial to Evaluate Preoperative Home-based Supervised Exercise Program for Prehabilitation of Frail Elderly Patients Undergoing Major Abdominal Surgery, Against Current Home-based Unsupervised Exercise Program.

Singapore General Hospital1 site in 1 country140 target enrollmentApril 10, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Frail Elderly Syndrome
Sponsor
Singapore General Hospital
Enrollment
140
Locations
1
Primary Endpoint
Change in functional walking capacity from baseline to just before surgery, as measured using the 6-minute walk distance.
Last Updated
4 years ago

Overview

Brief Summary

Singapore's population is ageing, and more elderly people are undergoing elective major surgeries. Frail elderly experience greater functional decline and slower recovery in physical function after surgery compared to non-frail elderly. Preoperative prehabilitation aims to enhance both aerobic capacity and physical strength of elderly to attenuate the post-operative decline in physical function. Singapore General Hospital has a bespoke preoperative program - Prehabilitation for Elderly Frail Patients Undergoing Elective Surgeries (PREPARE), where patients receive physiotherapy education and instructions for home-based unsupervised exercise program (uSEP). A hospital-based supervised exercise program had also been established but the take-up rate was low (7.6%) due to barriers such as cost and accessibility. Perioperative supervised exercise training can effect greater gains in functional capacity and muscle strength compared to no supervision. For the elderly with limited transport options to the hospital, home-based supervised programmes may be more convenient compared to hospital-based supervised programmes, but the former is costlier too. Home-interventions may also empower patients with the skills and confidence to maintain their physical fitness at home, which increases their likelihood of exercising after surgery.

The investigators propose a prospective single-center randomized controlled trial to evaluate the efficacy of preoperative prehabilitation with a home-based supervised exercise program (SEP) for frail elderly patients undergoing major abdominal surgery, compared to the mainstay of clinical practice, which is a home-based uSEP.

Registry
clinicaltrials.gov
Start Date
April 10, 2021
End Date
December 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Elective major abdominal surgery
  • Lead time \>= 14 days to surgery
  • Edmonton Frail Scale total score \>= 6 points or Functional performance score (Timed up and Go(TUG)) \>= 1 point

Exclusion Criteria

  • Inability to provide written informed consent due to cognitive impairment
  • Having Comorbid medical conditions interfering with the ability to perform exercise at home or to complete the testing procedures. These include: i. Unstable cardiac conditions ii. Acute illnesses iii. Patients who are completely unable to walk

Outcomes

Primary Outcomes

Change in functional walking capacity from baseline to just before surgery, as measured using the 6-minute walk distance.

Time Frame: From recruitment to 2-days before surgery

Distance that the patient can walk in 6 min, along a 15-20m hallway, at a pace that the participants will be tired at the end of the distance. This is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.

Secondary Outcomes

  • Hospital length-of-stay(From day of surgery until discharge, or up to 6 months after surgery, whichever occurs first)
  • Change in 6-minute walking distance(Day of recruitment, 2 days before surgery, 4 weeks and 8 weeks postoperative)
  • Maximal Inspiratory Pressure (MIP)(Day of recruitment, 2 days before surgery, 4 weeks and 8 weeks postoperative)
  • Handgrip strength (HGS)(Day of recruitment, 2 days before surgery, 4 weeks and 8 weeks postoperative)
  • 30-day in-hospital complications(From day of surgery to 30-days afterwards)
  • Health-related quality of life outcomes (HRQoL) as measured using the EQ-5D-3L(Day of recruitment, 2 days before surgery, 4 weeks, 8 weeks and 6 months postoperative)
  • Health-related quality of life outcomes (HRQoL) as measured using the 12-Item Short Form Survey (SF-12)(Day of recruitment, 2 days before surgery, 4 weeks, 8 weeks and 6 months postoperative)
  • 30-second and 1-minute Sit-to-Stands (STS)(Day of recruitment, 2 days before surgery, 4 weeks and 8 weeks postoperative)

Study Sites (1)

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