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Efficacy of Oral Nutritional Supplement in Community-Dwelling Adults Following Acute Care

NCT07753239 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 304

Last updated 2026-08-07

No results posted yet for this study

Summary

The study aims to determine the effects of Oral Nutritional Supplement (ONS) added to usual care on body weight compared with usual care alone in community-dwelling adults aged 55 years and older who are at risk of malnutrition and have low muscle strength following acute care.

Participants randomized to receive either ONS twice daily for 180 days plus usual care, or usual care alone. Usual care includes individualized dietary counseling and standardized physical activity advice provided. The study will assess body weight, nutritional status, muscle strength, physical function, dietary intake, and safety outcomes.

Conditions

  • Low Muscle Strength
  • Malnutrition

Interventions

DIETARY_SUPPLEMENT

ONS

230 mL per serving, twice daily

OTHER

Standard of Care (SOC)

Dietary counseling and physical activity advice

Sponsors & Collaborators

  • Abbott Nutrition

    lead INDUSTRY

Principal Investigators

  • Mandy Yen Ling Ow, Ph.D. · Abbott Nutrition

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
55 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-10-31
Primary Completion
2028-01-31
Completion
2028-01-31

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07753239 on ClinicalTrials.gov