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临床试验/NCT04851262
NCT04851262已完成不适用

Home-based Progressive Resistance Exercise to Enhance Physical Performance of Older Adults With Possible Sarcopenia

The University of Hong Kong1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2021年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
1
主要终点
Change in lower-limb muscle strength at 12 weeks from baseline

研究概览

简要总结

The overall aim of the proposed project is to improve muscle strength in older adults with possible sarcopenia by promoting home-based progressive resistance exercise. The target population for health talks is community-dwelling older adults. A Three monthly home-visits and weekly phone calls will be made. A waitlist randomised controlled trial will be conducted to evaluate effectiveness, and qualitative feedback will be collected from participants. A pilot study will be conducted first.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
65 Years 至 89 Years(Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •The inclusion criteria are:
  • •Aged 65-89;
  • •Possible sarcopenia (defined by AWGS 2019);
  • •No cognitive impairment (Abbreviated Mental Test score ≥8); and
  • •No communication problems.

排除标准

  • •having engaged in a structured exercise programme in the past 6 months or planning to do so within the intervention period;
  • •mobility-limiting injury of the hands or lower limbs, surgery or hospitalisation within the intervention period;
  • •contraindications such as musculoskeletal/cardiorespiratory disorders, or any advanced diseases that inhibit them from exercising.

研究组 & 干预措施

Intervention

Experimental

The intervention is a 12-week home-based resistance training programme with phased progression. The intervention will have three phases: (i) an initial phase focused on training the target muscle(s)/movements with minimal or no external weight; (ii) an intermediate phase targeting muscle strength with increased practice resistance; and (iii) an advanced phase targeting the further enhancement of muscle strength by challenging multiple muscle groups. Each phase will involve exercises targeting the trunk, back, hip, upper-limb and lower-limb muscles.

干预措施: Exercise (Behavioral)

Waitlist control

Other

The waitlist control participants will start the intervention 12 weeks after the baseline assessment.

干预措施: Exercise (Behavioral)

结局指标

主要结局

Change in lower-limb muscle strength at 12 weeks from baseline

时间窗: 12 weeks after baseline

Measured by Short Physical Performance Battery (SPPB), higher score indicates better performance

次要结局

  • Change in lower-limb muscle strength at 24 weeks from baseline(24 weeks after baseline)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Pui-Hing Chau

Associate Professor

The University of Hong Kong

研究点 (1)

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