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Effects of an intervention program in patients with swallowing difficulties and Parkinson's

Effects of an intervention program in dysphagic patients with dysphagia Parkinson's

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5ddt474
Enrollment
Unknown
Registered
2023-11-17
Start date
2023-11-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Deglutition Disorders

Interventions

Stratified randomization will be carried out, so that individuals with Parkinson's are randomly distributed into two groups (A or B), using an Excel® spreadsheet. The professional responsible for carr
E02.760.169.063.500.387

Sponsors

Universidade Federal do Rio Grande do Norte
Lead Sponsor
Hospital Universitário Onofre Lopes
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults treated at the Hospital Universitário Onofre Lopes (HUOL); aged >18 years; of both genders; diagnosed with Parkinson's; complaining of oropharyngeal dysphagia; who had not previously undergone speech therapy

Exclusion criteria

Exclusion criteria: Patients with coexistence of other neurological diseases; with head and neck cancer; tracheostomy users; using an alternative feeding route; those who are unable to follow commands

Design outcomes

Primary

MeasureTime frame
Evaluate the signs and symptoms of dysphagia through clinical speech therapy assessment with food offered at the beginning and end of the study;Evaluate the signs and symptoms of dysphagia through video endoscopy of swallowing with the offer of different food consistencies at the beginning and end of the study ;Assess quality of life related to swallowing through self-reported protocols

Secondary

MeasureTime frame
Evaluate isometric tongue pressure using the Iowa Oral Performance Instrument at the beginning and end of the study;Evaluate the vocal signal through an acoustic analysis of the Acoustic Voice Quality Index (AVQI) and Acoustic Brethiness Index (ABI) at the beginning and end of the study;Evaluate cough function through peak expiratory flow with the MicroLife PF100 portable device at the beginning and end of the study

Countries

Brazil

Contacts

Public ContactRamon Araújo

Universidade Federal do Rio Grande do Norte

ramon.pacheco.016@ufrn.edu.br+55 84 987253959

Outcome results

None listed

Source: REBEC (via WHO ICTRP)