ClinicalTrials.Veeva

Menu

Evaluation of Dysphagia in Patients Diagnosed With Parkinson's Disease by Ultrasound

B

Beylikduzu State Hospital

Status

Completed

Conditions

Parkinson Disease

Treatments

Diagnostic Test: Ultrasound evaluation

Study type

Observational

Funder types

Other

Identifiers

NCT06655727
BeylikduzuStateH5

Details and patient eligibility

About

The primary aim of this study is to perform an ultrasonographic swallowing assessment in Parkinson's patients and healthy volunteers and compare the findings with those from clinical swallowing evaluations. The secondary aim is to examine the relationship between dysphagia and functional status.

Full description

Thirty patients aged 40-80 years, diagnosed with idiopathic Parkinson's disease (Modified Hoehn-Yahr stage 1-3), and thirty healthy volunteers who either applied to the Physical Therapy and Rehabilitation outpatient clinic or received inpatient rehabilitation at Beylikdüzü State Hospital and Istanbul Physical Medicine and Rehabilitation Training and Research Hospital will be included in this study. At the start of the study, sociodemographic data of both patients and volunteers will be recorded. The Mini-Mental Test and the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) will be used to evaluate the mental and functional status of the patients diagnosed with Parkinson's disease. After the clinical dysphagia evaluation, the EAT-10 questionnaire will be administered to the participants. Following this, an ultrasonographic swallowing assessment will be performed on the participants. The ultrasonographic measurements will include tongue thickness (cm), resting distance between the mandible and hyoid (cm), shortest distance between the mandible and hyoid (cm), hyoid displacement (cm), hyoid displacement percentage, tongue thickness (cm) (with 5ml of water), resting distance between the mandible and hyoid (cm) (with 5ml of water), shortest distance between the mandible and hyoid (cm) (with 5ml of water), hyoid displacement (cm) (with 5ml of water), and hyoid displacement percentage (%) (with 5ml of water).

Enrollment

60 patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of idiopathic Parkinson's disease by a neurologist.
  • Being in stages 1-3 according to the Modified Hoehn-Yahr Staging Scale.
  • Scoring at least 24 on the Mini-Mental State Examination (MMSE).
  • Not having received any therapy or treatment affecting swallowing, other than routine medication for Parkinson's disease.

Exclusion criteria

  • Presence of head or neck cancer that could cause dysphagia.
  • History of radiotherapy or surgery in the head and neck region.
  • Diagnosis of vascular parkinsonism or stroke.
  • Presence of cardiopulmonary disease that could affect swallowing or breathing.
  • Having received voice or swallowing therapy in the last 6 months.
  • Presence of a diagnosed psychiatric disorder.

Trial design

60 participants in 2 patient groups

Parkinson disease group
Description:
Patients with Parkinson's disease
Treatment:
Diagnostic Test: Ultrasound evaluation
Control group
Description:
Healthy volunteers
Treatment:
Diagnostic Test: Ultrasound evaluation

Trial contacts and locations

1

Loading...

Central trial contact

Büşra Şirin Ahısha, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems