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Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic Surgical Patients

Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic Surgical Patients (HEROS) - a Pilot Interventional Cohort Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05344313
Acronym
HEROS
Enrollment
47
Registered
2022-04-25
Start date
2022-06-01
Completion date
2024-06-30
Last updated
2024-10-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty, Sarcopenia

Keywords

Nutrition, Prehabilitation, Surgery, Rehabilitation, Exercise, HMB

Brief summary

Aims: Clinical frailty severely impacts the physical, functional and physiological reserves necessary for the recovery after surgery. Sarcopenia, a multifactorial, multi-organ process which lead to loss of muscle mass over time, eventually resulting in clinical frailty. These 2 entities result in an increased morbidity and mortality from surgery. They also lead to a slower recovery from surgery with some patients never reaching baseline function after their surgery. It is, therefore, important to optimize patients with sarcopenia prior to surgery to reduce the incidence of morbidity and mortality. Nutrition and resistance training have been shown to be able to curb the effects of sarcopenia. However, the type and regime of nutrition is still unknown. Hypotheses: The study team hypothesize that Ensure Plus Advance + HMB (beta-hydoxy-beta-methylbutyrate) would reduce the amount of IMAT (inter and intramuscular adipose tissue) in sarocpaenic patients after 2-4 weeks of prehabilitation. This effect would be sustained even after surgery and would continue to improve up to 3-months post-surgery whilst participating in rehabilitation. Taking Ensure Plus Advance + HMB would also improve functional parameters after prehabilitation, ensure a similar QoL 1-month post-surgery even if biochemical parameters may not show a significant improvement. Methods: The investigators would be conducting a pilot interventional cohort with an institution with an established prehabilitation programme (SKH) to evaluate the effect of the use a high protein, high calorie oral nutritional supplement (ONS) with HMB on muscle quality, using a device with Automated Intelligence (AI), in sarcopenic patients undergoing gastrointestinal surgery. Primary outcomes will be changes in Intermuscular Adipose Tissue (IMAT) while secondary outcomes include changes in functional parameters, quality-of-life (QoL), surgical outcomes and biochemical results.

Interventions

DIETARY_SUPPLEMENTEnsure Plus Advance

as in the arm description of the intervention

Sponsors

Abbott
CollaboratorINDUSTRY
Sengkang General Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

interventional cohort study

Eligibility

Sex/Gender
ALL
Age
40 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

1. between 40-90 years old 2. are sarcopenia (defined by the Asian Workgroup of Sarcopenia 2019 definition) 3. due to undergo elective major gastrointestinal surgery 4. able to satisfy at least 2 weeks of prehabilitation before surgery 5. ambulant 6. able to comply with physiotherapy and dietician advice

Exclusion criteria

1. Are pregnant 2. Are prisoners 3. Intellectually, mentally or emotionally deemed not able to provide an informed consent and/or are unable to fill up the post-procedure questionnaires 4. Have disease conditions requiring emergent/semi-emergent operation 5. Diabetes on oral hyperglycemic agents (OHGA) 6. Chronic Kidney Disease (CKD) or End-stage Renal Failure (ESRF) 7. Unable to or decline assessment for sarcopenia

Design outcomes

Primary

MeasureTime frameDescription
change of Inter-muscular adipose tissue (%) between baseline and 1 day before surgery1 day before surgerychange of Inter-muscular adipose tissue (%) between baseline and 1 day before surgery

Secondary

MeasureTime frameDescription
Change of handgrip strength after the prehabilitation programme1 day before surgeryChange of handgrip strength after the prehabilitation programme
Change of gait speed after the prehabilitation programme1 day before surgeryChange of gait speed after the prehabilitation programme
change in average length of hospitalizationup to 30 days post surgerychange in average length of hospitalization
change of Inter-muscular adipose tissue (%) from pre-surgery to 3-months post-surgery3 months post surgerychange of Inter-muscular adipose tissue (%) from pre-surgery to 3-months post-surgery
change in quality of life measure (EuroQol-5D) at 1-, 2- and 3-months post-surgery1,2 and 3 months post surgerychange in quality of life measure (EuroQol-5D) at 1-, 2- and 3-months post-surgery

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026