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Clinical Trials/NCT04355299
NCT04355299
Completed
Not Applicable

Effectiveness of a Short-term Mixed Exercise Program for Treating Sarcopenia in Hospitalized Patients Aged 80 Years and Older

Yuxiang Liang0 sites121 target enrollmentOctober 1, 2016
ConditionsSarcopenia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sarcopenia
Sponsor
Yuxiang Liang
Enrollment
121
Primary Endpoint
The change of activities of daily living from the baseline to the end of the 2-week intervention
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Most previous clinical trials that addressed exercise for sarcopenic elderly subjects focused on community-dwelling older adults who were relatively healthy. There is a notable paucity of high-quality research investigating the effects and feasibility of exercise for hospitalized or institutionalized older people, who are generally frailer and more severe in functional impairment than those living in the community. Moreover, most reported exercise programs were of long-term duration, which typically lasted 3 to 6 months with two sessions per week. It remains unclear whether short-term exercise would be effective for treating sarcopenia. Therefore, the investigators aimed to assess the effectiveness of short-term exercise for treating sarcopenia in hospitalized older patients aged 80 years and over.

Registry
clinicaltrials.gov
Start Date
October 1, 2016
End Date
January 1, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Yuxiang Liang
Responsible Party
Sponsor Investigator
Principal Investigator

Yuxiang Liang

Physiotherapist

West China Hospital

Eligibility Criteria

Inclusion Criteria

  • aged ≥80 years;
  • being able to ambulate (assistance was acceptable);
  • being able to communicate and collaborate with the physiotherapist;
  • with sarcopenia defined by the AWGS criteria ;

Exclusion Criteria

  • terminal illness;
  • uncontrolled heart failure;
  • myocardial infarction within the past three months;
  • uncontrolled respiratory failure;
  • bone fractures within the past three months;
  • acute pulmonary embolism;
  • major surgery within the past three months;
  • uncontrolled arrhythmia;
  • refusal to participate in this study.

Outcomes

Primary Outcomes

The change of activities of daily living from the baseline to the end of the 2-week intervention

Time Frame: 2 weeks

Basic activities of daily living (BADL) assessed by Barthel Index. The total score for Barthel Index ranges from 0 (worst) to 100 (best) points.

Secondary Outcomes

  • The change of handgrip strength(2 weeks)
  • The change of gait speed(2 weeks)
  • The change of the score of Short Physical Performance Battery(2 weeks)
  • The change of the score of Timed Up and Go test(2 weeks)

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