Clinical trial · Observational
İnvestigation of the Effect of Neck Endurance on Swallowing and Directional Coordination in Head and Neck Cancer Patients
NCT07434245CI-TRIAL-00104008completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In the study, it was aimed to evaluate the relationship between dysphagia, which is one of the treatment complications, and the variables of respiratory performance, intraoral pressure and neck endura, and to look at the future work and rehabilitation methods of these evaluation outcomes from a different parameter.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Head and Neck Cancer | Malignant Head and Neck Neoplasm | ALIAS | 0.90 |
| Neck Muscle Issue | — | UNRESOLVED | — |
| Respiratory Function | — | UNRESOLVED | — |
| Swallowing Disorder | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fiberoptic Endoscopic Evaluate Swallowing | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Head and Neck Cancer Patients without Swallowing Disorder
- description
- This group has 0 between 3 score in EAT-10 Scale.
- interventionNames
- Diagnostic Test: Fiberoptic Endoscopic Evaluate Swallowing
- label
- Head and Neck Cancer Patients with Swallowing Disorder
- description
- This group has 4 between 40 score in EAT-10 Scale.
- interventionNames
- Diagnostic Test: Fiberoptic Endoscopic Evaluate Swallowing
Primary outcomes (5)
- measure
- FEES
- timeFrame
- through study completion, an average of 6 months.
- description
- Fiberoptic Endoscopic Evaluate Parametres ( PAS, Yale Residue Scale, Murray Secretion Scale)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Diagnosing head and neck cancer patients (larynx, nasopharynx, tongue, tonsil, parotid, retromolar trigone, lip, tongue root, hypopharyngeal cancers) * Statement with consent considering participating in the study * Disorders that cause obstacles due to the Function Test and intraoral passages Exclusion Criteria: * Presence of a chronic disease that prevents participation in the pulmonary function test and the study by the radiation oncology doctor and otolaryngologist. * Patients with swallowing problems due to previous illness or surgery * Acute surgical patient
References
Publications (0)
Data not yet available
No reference posted for this study.