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Non-sarcopenic SubjectsGSOMNCT07658612

Research on the Possible Relationship Between Sarcopenia and Oral Muscle Function

An observational study of Non-sarcopenic Subjects and Possible Sarcopenia, run by Chang Gung University of Science and Technology at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study will focus on community-dwelling elderly individuals and will follow the community screening process recommended by AWGS. It is expected to recruit 100 individuals who may have sarcopenia and 300 healthy or sub-healthy elderly individuals who are not likely to have sarcopenia, totaling 400… Read more about this study

Who is it for?
Ages 60 years and olderHealthy volunteers can take part
What is being tested?
Non interventional study
How many people
251 participants
Where
1 siteTaiwan
Study dates
14 Nov 2025to 4 Jun 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The research locations are the multimedia classroom on the 5th floor of the Department of Health and Nutrition at Chang Gung University, as well as community care centers in various districts of Taoyuan City and New Taipei City.

Case group - Inclusion Criteria:

  • aged 60 years (inclusive) or older
  • general public or residing in an institution for 3 months (inclusive) or more
  • willing to participate in the experimental design and sign the consent form
  • able to eat independently by mouth
  • identified by researchers as possibly having sarcopenia

Control group-Inclusion Criteria:

  • aged 60 years (inclusive) or older
  • general public or residing in an institution for 3 months (inclusive) or more ●willing to participate in the experimental design and sign the consent form
  • able to eat independently by mouth
  • identified by researchers as not possibly having sarcopenia

Case group 、Control group- Exclusion Criteria:

  • having comorbidities, critical illnesses, undergoing major surgeries, cancer, renal failure, liver failure, kidney diseases, liver diseases, having malignant tumors in the past five years, inflammation symptoms (C-reactive protein >10mg/dl)
  • severely malnourished individuals (GNRI < 82)
  • long-term tube-fed individuals.

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Chang Gung University of Science and Technology

    Taoyuan

Other trials in Taiwan

About this study

Official title: A Study on the Correlation Between the Genetic Polymorphisms of Elderly Individuals in the Community and Possible Sarcopenia and Oral Muscle Function

This study will focus on community-dwelling elderly individuals and will follow the community screening process recommended by AWGS.

It is expected to recruit 100 individuals who may have sarcopenia and 300 healthy or sub-healthy elderly individuals who are not likely to have sarcopenia, totaling 400 participants.Basic data such as age and body composition will be collected, as well as dietary records (three days), nutritional status assessments (Mini Nutritional Assessment, MNA), and oral health status records (including records of missing teeth, the number of opposing teeth, and whether participants wear fixed or removable dentures).

Read more

Chewing and swallowing abilities will be recorded using the Eating Assessment Tool (EAT-10). In a non-invasive manner, saliva samples will be collected for genomic DNA (gDNA) extraction, followed by quantitative gDNA typing analysis of seven gene loci (shown in Table 3).

Genotype data will be statistically analyzed along with participants' basic information, relevant sarcopenia screening data, and parameters related to oral health and swallowing function. This study adopts a case-control experimental design with the following objectives:

  1. to explore the incidence of possible sarcopenia in community-dwelling elderly.
  2. to investigate the relationship between oral function and possible sarcopenia in community-dwelling elderly using tongue pressure measurements.
  3. to understand the correlation between sarcopenia risk in community-dwelling elderly and seven specific genes.
  4. to examine the relationship between oral function and seven specific genes in community-dwelling elderly.
  5. to investigate the relationship between tongue pressure measurements and the values measured using edible chewing gum.
  6. to establish a standard test for evaluating oral chewing function using edible chewing gum.

By examining the possible mechanisms of the different genes involved in the causes of sarcopenia, we aim to find prevention strategies that are suitable for participants with different gene types.

Being tested
Non interventional study
Keywords
Genetic polymorphisms, Sarcopenia, Community-dwelling elderly, Chewing ability, Swallowing function, Genotype analysis
Medical subject headings
Sarcopenia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Non interventional studyOther

    NON

Study groups in NCT07658612
Study groupRoleWhat they receive
Case groupPossible sarcopenia
Receives: Other: Non interventional study
Control groupNon-possible sarcopenia
Receives: Other: Non interventional study

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Based on the results of empirical research on sarcopenia in Asian countries, a diagnostic consensus was established.

    • The cut-off point for abnormal grip strength is less than 28 kg for men and less than 18 kg for women
    • 6-meter walking speed less than 1.0 second/meter
    • 5-time chair stand test greater than or equal to 12 seconds
    • Short physical performance battery, SPPB greater than or equal to 9 points The above data will be combined to determine whether sarcopenia is possible

    Measured: baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jun 2026
  2. Study start14 Nov 2025
  3. Primary completion4 Jun 2026
  4. Study completion4 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
251 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07658612
Sponsor's protocol ID
202402045B0
Other IDs
NMRPF3Q0291
Acronym
GSOM
Status last verified
Jun 2026
First submitted
10 Jun 2026
Last updated
22 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Non-sarcopenic Subjects and Possible Sarcopenia, run by Chang Gung University of Science and Technology at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Based on the results of empirical research on sarcopenia in Asian countries, a diagnostic consensus was established. (time frame: baseline). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2026.

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