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Efficacy of LINE-Delivered Video Instructions Versus Educational Pamphlet for Swallowing Exercises in Stroke Patients with Dysphagia: A Randomized Controlled Trial

Efficacy of LINE-Delivered Video Instructions Versus Educational Pamphlet for Swallowing Exercises in Stroke Patients with Dysphagia: A Randomized Controlled Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260505002
Enrollment
40
Registered
2026-05-05
Start date
2026-05-12
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Post-stroke dysphagia Dysphagia Stroke Swallowing exercise Video instructions

Interventions

Patients receive standard care, an educational pamphlet for swallowing exercises, a logbook, and face-to-face instruction (1 session). Additionally, they receive a daily LINE message containing a vide
Experimental Other,Active Comparator Other
LINE-Delivered Video Instructions + Educational Pamphlet,Educational Pamphlet

Sponsors

Kabinburi Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years with confirmed ischemic or hemorrhagic stroke via CT or MRI. 2.Clinical signs of dysphagia confirmed by a baseline GUSS score < 20. 3.Good consciousness, stable vital signs, and ability to follow 2-step basic commands. 4.Patient or primary caregiver owns a smartphone with the LINE application installed, internet access, and the ability to play videos. 5.Provided signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Dysphagia caused by conditions other than the current stroke (e.g., neuromuscular disease, head/neck cancer, history of radiation, or esophageal structural abnormalities). 2.Patients with a tracheostomy. 3.Severe communication or language deficits (Severe aphasia). 4.Severe uncontrolled comorbidities (e.g., critical heart failure, sepsis, or ventilator dependence). 5.Pneumonia or active respiratory tract infection. 6.Severe visual or hearing impairment that prevents reading or watching videos on the LINE application. 7.End-of-life or receiving palliative care. 8.History of receiving swallowing rehabilitation from an occupational therapist within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Swallowing performance At 4 weeks Gugging Swallowing Screen (GUSS) score.

Secondary

MeasureTime frame
Adherence rate to the swallowing exercise program At 4 weeks. Percentage of completed exercise sessions recorded in the logbook,User experience regarding confidence, convenience, and usefulness of LINE reminders At 4 weeks. A 5-point rating scale questionnaire - Intervention group only

Countries

Thailand

Contacts

Public ContactSuthida Somnam

Kabinburi Hospital

kabinburihospital2567@gmail.com037288196

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026