- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05939908
Assessment of Hand Grip Strength Using Jamar Dynamometer
To Assess Prevalence of Sarcopenia Using Hand Grip Strength (HGS) as a Marker in Patients With T2DM
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Sarcopenia is an age related, progressive, and generalized skeletal muscle disorder involving the accelerated loss of muscle mass and function and physical performance below a defined threshold1. It is associated with increased adverse outcomes including increased risk falls, physical frailty, prolonged hospitalization, dependency, physical disability and impairment, limitation of mobility, decreased quality of life and increased mortality. Sarcopenia is known to be more prevalent in older populations, but the decline in muscle mass starts from ~40 years onwards2.
Sarcopenia not only affects the ability to lead an active lifestyle but also contributes to increased obesity, type 2 diabetes (T2DM) reduced quality of life, osteoporosis, and metabolic health1.
Hand grip strength (HGS) is considered as an important value when diagnosing sarcopenia. Lower muscle strength using HGS is mandatory to diagnose sarcopenia. EWGSOP group recommends that the mean reference cut-off value of hand grip is < 30 kg in men and < 20 kg in women.
There is evidence that strength could be an important risk factor for diabetes. Low hand-grip strength has been predictive of incident diabetes in prospective cohort studies3. Lower grip strength was associated with higher prevalence of diabetes, independent of confounding factors, across all ethnicities in both men and women. Diabetes prevalence was approximately three- to fourfold higher in South Asian participants across all levels of grip strength3 .
However, there are no studies in India assessing sarcopenia in type 2 diabetic patients.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Anoop Misra, MD
- Phone Number: 01149101222
- Email: anoopmisra@gmail.com
Study Contact Backup
- Name: Bhavya Arora, M.Sc
- Phone Number: 01149101222
- Email: bhavyam_1010@yahoo.co.in
Study Locations
-
-
-
Delhi, India, 110048
- Recruiting
- Fortis CDOC Hospital
-
Principal Investigator:
- Anoop Misra, MD
-
Contact:
- Anoop Misra, MD
- Phone Number: 01149101222
- Email: anoopmisra@gmail.com
-
Sub-Investigator:
- Bhavya Arora, M.Sc
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
All patients with Type 2 diabetes of any duration coming for first time in OPD
Exclusion Criteria:
- Patients with hand fracture
- Thyroid dysfunction
- Any musculoskeletal condition causing difficulty in holding the dynamometer
- Patients with type1 diabetes (T1DM) and gestational diabetes (GDM)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Comparison of age and gender specific prevalence of sarcopenia using HGS in patients with T2DM
Time Frame: 6 days
|
6 days
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Anoop Misra, MD, Fortis CDOC Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HGS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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