Effects of CTAR and a Swallowing Pressure Ball in Older Stroke Adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial examines a 12-week home-care swallowing rehabilitation program combining Chin Tuck Against Resistance (CTAR) and a swallowing pressure ball versus conventional swallowing rehabilitation in older adults with post-stroke dysphagia. Participants are adults aged 65–90 who had an ischemic or hemorrhagic stroke more than 6 months ago and are receiving home care. Outcomes include standardized swallowing assessments, quality of life related to swallowing, and adherence to the rehabilitation protocol. The trial aims to assess feasibility and potential clinical benefits of resistance-based, home-based swallowing rehabilitation in community settings.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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.

Where it's running

• ChiMei Medical Center
  Tainan, Tainan City, Taiwan Recruiting

Study contacts

• Study coordinator: nai ching Chen, RN
• Email: dreampatty11@gmail.com
• Phone: +886 988031533

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  Recruiting Phase 2 Hokkaido University Hospital · Sapporo, Hokkaido · NCT06752720

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.