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The Effect of an Auditory Rhythmic Cue on the Frequency of Rolling in Patients With Dysphagia and Parkinson's Disease: a Pilot Study

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT06695455
Title field or adapter rule
{'original_value': "The Effect of an Auditory Rhythmic Cue on the Frequency of Rolling in Patients With Dysphagia and Parkinson's Disease: a Pilot Study", 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At
2026-10-31T23:27:33.283331+00:00
Published At
2026-10-30T00:00:00+00:00
Record Updated At
2026-10-30
Source Retrieved At
2026-10-31T22:18:37.902788+00:00
Timestamp Basis
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Oral Festination", "Lingual Pumping", "Dysphagia", "Swallowing Disorder", "PARKINSON DISEASE (Disorder)"]
protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-30", "type": "ACTUAL"}
protocolSection.identificationModule.nctId
"NCT06695455"
protocolSection.identificationModule.officialTitle
"The Effect of an Auditory Rhythmic Cue on the Frequency of Rolling in Patients With Dysphagia and Parkinson\u0027s Disease: a Pilot Study"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct
null

Study condition terms

  • Oral Festination (protocolSection.conditionsModule.conditions)
  • Lingual Pumping (protocolSection.conditionsModule.conditions)
  • Dysphagia (protocolSection.conditionsModule.conditions)
  • Swallowing Disorder (protocolSection.conditionsModule.conditions)
  • PARKINSON DISEASE (Disorder) (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

  • {'armGroupLabels': ['experimental arm - dysphagic parkinson patient'], 'description': 'Three assessments, each spread over two days, will be administered at three different time points during the study: before the experiment (T0), after 7 weeks of the experiment (T1), and 3 months after the intervention (T2). The evaluation will include a pharyngography as well as a clinical assessment of swallowing and rhythmic abilities.\n\nEach subject will be invited to participate in 3 individual rehabilitation sessions per week for 7 weeks, conducted by a speech therapist at La Musse Hospital. Each session will be structured similarly: the subject will be asked to swallow their saliva, followed by a nectar-like texture (IDDSI 2) and a pudding-like texture (IDDSI 4), timed to the rhythm of a metronome. The rhythm will vary throughout the sessions. The goal will be to get as close as possible to the rhythm of a healthy swallow.', 'name': 'Swallowing rehabilitation by rhythmic auditory cue', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.