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临床试验/NCT06337357
NCT06337357招募中不适用

Evaluating Resistance Training for Sarcopenia in Older Patients With Type 2 Diabetes: Treatment Outcomes

National Geriatric Hospital2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
80
试验地点
2
主要终点
Muscle mass

研究概览

简要总结

A randomized controlled clinical trial that will test how progressive resistance training will impact outcomes of sarcopenia in older patients with type 2 diabetes who have been diagnosed as sarcopenia. The intervention will be 12 weeks in duration with approximately 24 sessions of resistance exercises. Outcome measures will be collected at baseline, 4, 8 weeks and 12 weeks.

详细描述

Sarcopenia, prevalent among geriatric populations, involves the progressive loss of muscle mass and decline in muscular function. This age-related condition is associated with higher susceptibility to falls, comorbidities, and mortality. Resistance training emerges as a non-pharmacological intervention proven to alleviate and potentially delay the progression of sarcopenia. However, there are still few studies investigating its effects on outcomes in older patients with diabetes mellitus.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
60 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Type 2 diabetic patients diagnosed using American Diabetes Association 2022 criteria
  • HbA1c ≥ 7.0 and ≤ 8.5%
  • Sarcopenia diagnosed using criteria from the Asian Working Group for Sarcopenia 2019
  • Age ≥ 60 and ≤ 80

排除标准

  • Acute diabetic complications
  • Patients are in the acute phase of musculoskeletal disorders: acute gout, progressing low-grade arthritis, acute joint pain due to joint degeneration, sciatic pain, and infectious arthritis.
  • Patients suffer from conditions significantly affecting cognition and mobility: sequelae of stroke (with weakness, limb paralysis), muscular weakness, limb disabilities, severe heart failure, severe cognitive decline, and psychiatric disorders.
  • Patients have been bedridden due to illness for more than 1 month within the past 3 months up to the recruitment time.
  • Patients with cardiovascular diseases: chest pain, uncontrolled blood pressure ≥160/100 mmHg, untreated cardiac arrhythmia, a history of congestive heart failure, severe valvular heart disease, myocarditis or pericarditis, and hypertrophic cardiomyopathy.
  • Renal failure with estimated glomerular function rate (Modification of Diet in Renal Disease equation) < 60 ml/min/m3 or serum creatinine ≥ 130 µmol/l
  • On treatment with Sodium-glucose cotransporter 2 inhibitors (SGLT2i)

结局指标

主要结局

Muscle mass

时间窗: Prior to the start of intervention, after 4 weeks, 8 weeks and 12 weeks (completion of the intervention)

Upper and lower muscle mass are measured by Bioelectrical impedance analysis (BIA) method, using a machine model named InBody 770: the higher number the better outcome.

Physical performance 1 - Handgrip strength

时间窗: Prior to the start of intervention, after 4 weeks, 8 weeks and 12 weeks (completion of the intervention)

Handgrip strength is assessed using a hand dynamometer named Jamar Hydraulic Hand Dynamometer: the higher number the better outcome.

Physical performance 2 - Gait speed

时间窗: Prior to the start of intervention, after 4 weeks, 8 weeks and 12 weeks (completion of the intervention)

4-metre gait speed test (the shorter time the better outcome)

Physical performance 3 - Short Physical Performance Battery (SPPB)

时间窗: Prior to the start of intervention, after 4 weeks, 8 weeks and 12 weeks (completion of the intervention)

The Short Physical Performance Battery developed by the National Institute on Aging: scores ranging from 0 (worst) to 12 (best)

次要结局

  • Health-related Quality of Life(Prior to the start of intervention (Week 0), following the completion of the intervention (Week 12))
  • Activities of Daily Living (ADLs) and Instrumental Activities of Daily Living (IADLs)(Prior to the start of intervention (Week 0), following the completion of the intervention (Week 12))
  • Nutritional status(Prior to the start of intervention (Week 0), following the completion of the intervention (Week 12))

研究者

发起方
National Geriatric Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Trinh Ngoc Anh

Endocrinologist, Principal Investigator and Sponsor

National Geriatric Hospital

研究点 (2)

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