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The Effects of A Neurospeech-based Training System on Elderly Patients with Speech Disorders: An Exploratory Randomized Controlled Study

The Effects of A Neurospeech-based Training System on Elderly Patients with Speech Disorders: An Exploratory Randomized Controlled Study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098227
Enrollment
Unknown
Registered
2025-03-04
Start date
2025-06-09
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

speech disorder

Interventions

treatment group:This study will distribute a tablet with the same brand and model to each patient in the home treatment group before the start of treatment. The device name and model are Huawei Glory
control group:Patients in the control group did not receive any form of speech rehabilitation treatment for four weeks during the study period, and were only given health guidance

Sponsors

Beijing Rehabilitation Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1 Age ranged from 60 to 85 years; 2 Diagnosed by a clinician or therapist with speech disorders or complained of speech problems such as abnormal arthria and reduced vocalization; 3 Junior high school education or above; 4 Be able to learn independently or use a tablet computer with the help of family members and caregivers for home language training; 5 Living in Beijing for a long time or during the study period.

Exclusion criteria

Exclusion criteria: 1 Patients with speech disorders and combined aphasia symptoms; 2 Suffering from Alzheimer's disease or severe cognitive impairment and other major mental illnesses; 3 Those who have severe visual/hearing impairment and are unable to cooperate to complete the study; 4 Previous history of throat tumors or throat and vocal cord surgeries; 5 Unable to cooperate in completing the study or unwilling to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
the score of modified Frenchay Dysarthria Assessment;

Secondary

MeasureTime frame
Voice Handicap Index;The Mann Assessment of Swallowing Ability;

Countries

China

Contacts

Public ContactBoyan Fang

Beijing Rehabilitation Hospital Affiliated to Capital Medical University

fangboyanv@ccmu.edu.cn+86 188 0108 6480

Outcome results

None listed

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