跳至主要内容
临床试验/NCT07620210
NCT07620210招募中不适用

Effectiveness of Combining Chin Tuck Against Resistance Swallowing Training and an Innovative Swallowing Pressure Measurement Ball on the Swallowing Function and Quality of Life in Home-Based Older Adults With Stroke

Chimei Medical Center1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2026年3月18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
132
试验地点
1

研究概览

简要总结

This study aims to investigate the effectiveness of resistance swallowing rehabilitation using Chin Tuck Against Resistance (CTAR) exercises combined with an innovative swallowing pressure ball in improving swallowing function and swallowing-related quality of life among home-based older stroke patients with dysphagia.

Participants will receive a 12-week swallowing rehabilitation program conducted in the home-care setting. Outcome measures include swallowing function assessments, swallowing-related quality of life, and rehabilitation adherence. The study is designed as a randomized controlled trial to explore the feasibility and clinical benefits of resistance-based swallowing rehabilitation in community and home-care environments.

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
65 Years 至 90 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 65 and 90 years.
  • Diagnosed with ischemic or hemorrhagic stroke more than 6 months prior to enrollment.
  • Receiving home care services from participating home care agencies.
  • Able to follow instructions and participate in swallowing training.
  • MMSE score ≥24, or adjusted according to education level.
  • Passed the second stage of the 3-step swallowing screening test.
  • Presence of post-stroke dysphagia symptoms.

排除标准

  • History of head and neck cancer or head and neck radiotherapy.
  • History of cervical spine surgery or tracheostomy.
  • Severe neurological or neuromuscular diseases affecting swallowing function.
  • Severe unstable medical conditions.
  • Current use of medications significantly affecting swallowing function or muscle tone.
  • Unable to complete the intervention or follow-up assessments.
  • Receiving tube feeding without oral intake ability.

研究者

发起方
Chimei Medical Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

NAI CHING CHEN

Principal Investigator

Chimei Medical Center

研究点 (1)

Loading locations...

相似试验