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NCT06527742Completed

Body Composition, Frailty, and Function in Rehabilitation

Correlations of Body Composition Measures With Functional Outcomes and the Clinical Frailty Scale in Inpatient Rehabilitation: A Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 29 Oct 2026

Brief summary (registry, in English)

The investigators are investigating if body composition measures - in particular muscle mass, body fat, and something called the phase angle - are able to reliably predict functional outcomes for patients who are in an acute hospital for inpatient rehabilitation. The investigators also want to see if age and frailty affect these relationships. Patients undergoing inpatient rehabilitation in our hospital will be monitored through a variety of frailty-specific tools, including strength and speed. The investigators will use a device called a body composition monitor (BCM) to record their body composition measurements. These will then be compared against their usual rehabilitation outcomes. The investigators believe that there is a correlation between these measures and a patient's functional outcomes.

Status (registry)
Completed
Study type
Observational
Enrollment
345 (actual)
First submitted
16 Jul 2024
Start date
9 Dec 2024
Primary completion date
12 Dec 2025
Lead sponsor
Changi General Hospital
Diseases
Stroke
NCT number
NCT06527742

What you commit to

  • Study type: Observational
  • Participants enrolled: 345
  • From 9 Dec 2024 to the primary completion date, 12 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Medical devices or surgical implants that will interfere with BIA measurement per the manufacturer's guidelines

Other

  • Pacemaker or implantable defibrillator in-situ
  • Abnormal fluid status (overloaded or depleted) at the point of screening
  • Cognitive or physical inability to tolerate sitting/lying still for 2mins (for BIA measurement)

Who the study is looking for

  • Transferred under the Rehabilitation Medicine service for post-acute rehabilitation
  • Rehabilitation diagnosis of:
    • Stroke with motor weakness (modified Rankin scale 1-5), or
    • Deconditioning (from sepsis, post-ICU admission, heart failure, falls, musculoskeletal conditions with or without pain, or other conditions), or
    • Pulmonary rehabilitation (with or with long-term oxygen therapy), or
    • Lower limb amputees (transtibial or transfemoral)
  • Medically stable
  • Able to understand English consent form or suitably-translated document, or have a family member/legally-authorised representative who is able to do so and willing to provide consent

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Changi General Hospital
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.