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N/A N=95 Randomized Single-blind Basic Science

Identifying Therapeutic Targets of Accelerated Sarcopenia

Sarcopenia · Diabetes Mellitus · Aging

Enrolled (actual)
95
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcome: Primary: Leg Lean Mass — 0.35; -0.55; -0.80; -0.44 kg — p=<0.01

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Resistance exercise training (Behavioral); Bed rest (Behavioral); Intensive physical therapy (Behavioral)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
The University of Texas Medical Branch, Galveston
Primary completion
Aug 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Leg Lean Mass
0.35; -0.55; -0.80; -0.44; -0.66; -0.59 <0.01 sig
SECONDARY
Knee Extension Strength
3; -12; -24; -23; -30; -14 <0.01 sig

Summary

The proposed research is designed to identify the mechanisms that can accelerate loss of muscle size, strength and physical function in type 2 diabetes and with hospitalization in older persons. About ⅓ of older Americans have type 2 diabetes, and about ⅓ of the hospitalizations in the USA involve persons older than 65 year of age. The proposed research is relevant to the part of NIH's mission that pertains to development of the fundamental knowledge that will improve health and reduce the burdens of disability, because this work will provide the fundamental evidence to identify new targets for the development of innovative treatments to slow down muscle loss and disability in our aging society.

Eligibility Criteria

Inclusion Criteria

  • Body mass index: 8%
  • Impairment in Activities of Daily Living
  • >2 falls/year
  • weight loss >5% in the past 6 months
  • Exercise training (≥2 sessions/week) or ≥10, 000 steps/day
  • Significant cardiovascular, liver, renal, blood, or respiratory disease
  • Active cancer or infection
  • Recent (within 3 months) treatment with anabolic steroids, systemic corticosteroids or estrogen.
  • Alcohol or drug abuse
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03118050). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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