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Health and Nutrition Status of Chinese Elderly

Health Status of Chinese Elderly

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02089906
Enrollment
2834
Registered
2014-03-18
Start date
2014-03-31
Completion date
2015-07-31
Last updated
2015-08-04

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

Conditions

Malnutrition, Sarcopenia

Brief summary

This study is aiming to understand the prevalence and risk factors related to malnutrition and sarcopenia in Chinese elderly.

Detailed description

The study objective is to understand the prevalence of malnutrition and sarcopenia in Chinese elderly with the cut-off points from the normal range of muscle mass and function in Chinese adults; to understand the risk factors related to malnutrition and sarcopenia in Chinese elderly; to set up a screening tool on malnutrition and sarcopenia risks in Chinese elderly.

Interventions

None listed

Sponsors

Abbott Nutrition
Lead SponsorINDUSTRY

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Male or female Chinese ages \>= 60 years. 2. Subject lives in the community for more than 12 months. 3. Subject has voluntarily signed and dated an informed consent form, approved by an Independent Ethics Committee/Institutional Review Board (IEC/IRB) prior to any participation in the study.

Exclusion criteria

1. Subject who did/does heavy manual labor 2. Subject who was a professional or semi-professional athlete or game player 3. Subject who has physical disabilities such as loss of hand or foot or limbs or any other physical disability which may affect the muscle mass by the opinion of the study physician. 4. Subject has an implanted electronic device or orthopedic metal implantations, such as pacemaker, cardiac defibrillator, subcutaneous injection pump, or metal hip, metal knee joint, metal fracture internal fixation, etc. 5. Subject who has active hyperthyroidism or hypothyroidism and needs medication treatment as by self-report. 6. Subject who has severe heart dysfunction or renal dysfunction with significant sodium water retention or edema by the opinion of study physicians. 7. Subject who takes hormones except for external application of glucocorticoids. 8. Subject who takes diuretics except for using a stable dose for at least 3 weeks as a part of hypertension treatment. 9. Subject who has later stage of malignancies with cachexia by the opinion of study physicians. 10. Subject has any other disease or situation who should not to participate in the study by the opinion of study physicians. 11. Subject had hand/wrist or foot/leg surgery/injury within the past 3 months and the surgery/injury may affect the hand grip or gait speed test by study physician's opinion. 12. Subject is too frail by study physician's opinion 13. Subject is drug addicted or alcohol addicted 14. Subject is participating in other clinical trials which are not approved by AN

Design outcomes

Primary

MeasureTime frameDescription
Total skeletal muscle massTest Visit 1 (~ Day 7)bioelectric impedance absorptiometry (BIA)

Secondary

MeasureTime frameDescription
Total skeletal muscle massTest Visit 2 (~ Day 17)Dual X-ray Absorptiometry (DXA)
Total body fatTest Visit 1 (~Day 7) and Test Visit 2 (~ Day 17)
Hand grip strengthTest Visit 1 (~ Day 7)
Gait speedTest Visit 1 (~ Day 7)
Total body fat free massTest Visit 1 (~ Day 7) and Test Visit 2 (~ Day 17)

Countries

China

Outcome results

None listed

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