Case Control in Sarcopenia Among Elderly Type 2 Diabetic Patients

December 18, 2025 updated by: Eman Alaa Eldean Mohamed

Asessment of Sarcopenia Among Elderly Type 2 Diabetic Patients

  1. Assess sarcopenia prevalence in elderly diabetic patients.
  2. Evaluate impact of diabetes and its medications on muscle health.
  3. detect effect of sacropenia on quality of life on elderly

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

  1. Inclusion criteria:

    The study will included all patient ,age ≥ 60 years,diagnosed with type 2 diabetes mellitus at least 5 years duraation according to ADA guideline referance(8) (diabetes can be made if a patient's A1C is 6.5% or higher, their FPG is 126 mg/dL or higher, or their 2-hour plasma glucose during an OGTT is 200 mg/dL or higher. A random plasma glucose of 200 mg/dL or higher, in conjunction with classic symptoms of hyperglycemia, also indicates diabetes)

    ●Able to give informed consent

  2. Exclusion criteria:

    • chronic renal disease
    • chronic liver disese
    • Severe cognitive impairment
    • Known neuromuscular diseases affecting mobility
    • malignancy Data of the study will collected over one year duration from 1/2026 _1/2027

Description

  1. Inclusion criteria:

    The study will included all patient ,age ≥ 60 years,diagnosed with type 2 diabetes mellitus at least 5 years duraation according to ADA guideline referance(8) (diabetes can be made if a patient's A1C is 6.5% or higher, their FPG is 126 mg/dL or higher, or their 2-hour plasma glucose during an OGTT is 200 mg/dL or higher. A random plasma glucose of 200 mg/dL or higher, in conjunction with classic symptoms of hyperglycemia, also indicates diabetes)

    ●Able to give informed consent

  2. Exclusion criteria:

    • chronic renal disease
    • chronic liver disese
    • Severe cognitive impairment
    • Known neuromuscular diseases affecting mobility
    • malignancy Data of the study will collected over one year duration from 1/2026 _1/2027

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Diabetic Group
Elderly patients with type 2 diabetes mellitus. Participants will be evaluated for the presence or absence of sarcopenia using muscle ultrasound and clinical criteria.
Bedside muscle ultrasound to measure muscle thickness, cross-sectional area and echogenicity
Non-Diabetic Group
Elderly patients without diabetes mellitus. Participants will also be assessed for sarcopenia using muscle ultrasound and standard diagnostic criteria.
Bedside muscle ultrasound to measure muscle thickness, cross-sectional area and echogenicity

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of sarcopenia assessed by muscle ultrasound in elderly diabetic
Time Frame: Within 6 months from the start of recruitment.
Sarcopenia will be evaluated using muscle ultrasound to measure muscle thickness and echo intensity of the quadriceps muscle. The results will be interpreted according to EWGSOP2 diagnostic criteria, which combine muscle mass and muscle strength parameters
Within 6 months from the start of recruitment.
Assessment of muscle strength using handgrip dynamometry
Time Frame: Within 6 months
Handgrip strength will be measured using a handheld dynamometer, and the average of three attempts for the dominant hand will be recorded.
Within 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of life score using the SarQoL questionnaire.
Time Frame: Within 6 months.
Quality of life related to sarcopenia will be evaluated using the validated SarQoL questionnaire.
Within 6 months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 22, 2025

Primary Completion (Estimated)

October 20, 2027

Study Completion (Estimated)

October 20, 2028

Study Registration Dates

First Submitted

September 23, 2025

First Submitted That Met QC Criteria

November 20, 2025

First Posted (Estimated)

November 24, 2025

Study Record Updates

Last Update Posted (Actual)

December 19, 2025

Last Update Submitted That Met QC Criteria

December 18, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

Yes

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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