Skip to content

Effect of group rehabilitation model on swallowing function, depression symptoms and quality of life of stroke patients with dysphagia: a randomized controlled trial

Effect of group rehabilitation model on swallowing function, depression symptoms and quality of life of stroke patients with dysphagia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056768
Enrollment
Unknown
Registered
2022-02-15
Start date
2021-08-15
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

Dysphagia after stroke

Interventions

intervention group:Group rehabilitation training

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria included: (1) Diagnosis of a cerebral hemorrhage or cerebral infarction according to World Health Organization (WHO)’s definition on stroke. Besides, the patients had to have first onset of the disease (course of disease: 5s), III, IV, and V on Water Swallowing Test; (4) Patients with suspected swallowing impairments detected by Water Swallowing Test were supposed to do the Videofluoroscopic swallowing study (VFSS) or Fiberoptic endoscopic evaluation of swallowing (FEES), further confirm that the patients does have dysphagia; (5) Understand brief functional instructions and coordinate with rehabilitation and evaluation. All the participants or their families gave informed written consent to the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria included: (1) Patients with difficulty following instructions or unable to complete the entire rehabilitation training process because of aphasia or cognitive impairment; (2) Complicated with severe cardiovascular disease or deterioration of respiratory function; (3) Preexisting diseases affecting swallowing function (such as Parkinson's disease or motor neuron disease), history of swallowing treatment or history of radiotherapy and chemotherapy in head and neck.

Design outcomes

Primary

MeasureTime frame
Functional Oral Intake Scale;Standardized Swallowing Assessment;

Secondary

MeasureTime frame
15-item Geriatric Depression Scale;Swallowing-related Quality of Life;

Countries

Guangdong

Contacts

Public ContactXieChunqing

The Third Affiliated Hospital of Sun Yat-sen University

370545760@qq.com+86 15246114536

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026