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Evaluation of the Effects of Preference-Oriented Dietary Modification on Swallowing Function in Acute Elderly Stroke Patients

Evaluation of the Effects of Preference-Oriented Dietary Modification on Swallowing Function in Acute Elderly Stroke Patients - Evaluation of the Effects of Preference-Oriented Dietary Modification on Swallowing Function in Acute Elderly Stroke Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057734
Enrollment
60
Registered
2025-07-01
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute stroke

Interventions

Dining,Selection of 10 commercially available seasonings to suit your tastes For both the intervention and control groups, the standard frequency and duration of swallowing training will be &quot
20 minutes per session, at least 5 times per week&quot
and will be standardized for both groups.In addition, the method of talking to and assisting the patients during the training will be uniformly applied in both groups. Regular meals served

Sponsors

Niigata University Regional Medical Education Center Uonuma kikan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with swallowing dysfunction (MASA score of 177 or less) as determined by our swallowing evaluation protocol. 2. Patients who are 65 years of age or older at the time of obtaining consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients who could not be assessed for swallowing function within 48 hours of onset 2. Patients with severe impaired consciousness, severe cognitive decline, or severe aphasia that would make intervention difficult and would make cooperation in the study difficult 3. Patients who will receive central venous nutrition with meals during the study period 4. Patients with diagnosis of lacunar infarction or subarachnoid hemorrhage (to limit stroke classification) 5. Patients with a history of dysphagia or a history of high risk of developing dysphagia (e.g., stroke, aspiration pneumonia, neuromuscular disease) 6. Patients whose general condition is poor and for whom it is deemed difficult to obtain the established assessment items 7. Patients with the following food allergies: shrimp, wheat, sesame, soybean, apple *Allergens contained in seasonings

Design outcomes

Primary

MeasureTime frame
1.The Mann Assessment of Swallowing Ability (MASA) 2.Functional Oral Intake Scale (FOIS), Oral Nutritional Intake 3.Simplified Nutritional Appetite Questionnaire-Japanese (SNAQ-J) Baseline, Week1, Week2, Week3, Discharge

Secondary

MeasureTime frame
Basic information: disease information, age, gender, complications, medical history, hospitalization, hospital stay, medications, etc. Biochemical data: ALB, WBC, CRP, BUN, Cre, Tf, Pre-ALB, etc. Vital data: temperature, blood pressure, blood oxygen saturation, heart rate, pulse rate, etc. Physical function: grip strength, tongue pressure, Barthel Index, Inbody, physical and cerebral palsy symptoms, etc. Imaging data: CT, MRI, VE, VF, chest X-ray, etc. Nutritional status: BMI, GNRI, CRP, Tf, Pre ALB, etc. Cognitive function: MMSE, presence of dementia, etc.

Countries

Japan

Contacts

Public ContactYuichiro Yoneoka

Niigata University Regional Medical Education Center Uonuma kikan Hospital neurosurgery

yone.bri@niigata-u.ac.jp025-777-3200

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026