NCT07620210 Effects of CTAR and a Swallowing Pressure Ball in Older Stroke Adults
| NCT ID | NCT07620210 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Chimei Medical Center |
| Condition | Stroke |
| Study Type | INTERVENTIONAL |
| Enrollment | 132 participants |
| Start Date | 2026-03-18 |
| Primary Completion | 2026-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 132 participants in total. It began in 2026-03-18 with a primary completion date of 2026-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
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.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07620210 clinical trial?
This trial is open to participants of all sexes, aged 65 Years or older, up to 90 Years, studying Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07620210 currently recruiting?
Yes, NCT07620210 is actively recruiting participants. Contact the research team at dreampatty11@gmail.com for enrollment information.
Where is the NCT07620210 trial being conducted?
This trial is being conducted at Tainan, Taiwan.
Who is sponsoring the NCT07620210 clinical trial?
NCT07620210 is sponsored by Chimei Medical Center. The trial plans to enroll 132 participants.
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