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Not yet recruiting NCT07320820

Quality of Life and Functional Outcomes in Laryngeal Cancer Patients

Conditions: Laryngeal Carcinoma Quality of Life (QOL) Patient Satisfaction Voice Quality Swallowing Function Pain Management Anxiety Depression

Sponsor: Saglik Bilimleri Universitesi

trial.available_in: БГ
Overview
Laryngeal squamous cell carcinomas are head and neck malignancies that directly affect both swallowing and voice functions and are associated with a significant deterioration in patients' quality of life throughout the treatment process. The aim of this study is to evaluate quality of life, voice and swallowing functions, pain, anxiety-depression levels, and patient satisfaction at the pre-treatment period and at the 3rd, 6th, and 12th months post-treatment in patients with laryngeal malignancies, using validated questionnaires, in order to: Elucidate the course of functional recovery following treatment, Individualize rehabilitation and follow-up strategies, and Examine the relationship between functional outcomes and oncological survival.
Who can participate
Inclusion Criteria: * Age ≥ 18 years at the time of enrollment. * Histopathologically confirmed diagnosis of laryngeal squamous cell carcinoma. * Planned to undergo surgical treatment or radiotherapy/chemoradiotherapy as part of standard oncological care. * Willing and able to participate in the study and to provide written informed consent. * No history of psychiatric or neurological disorders that could impair comprehension, questionnaire completion, or study participation. Exclusion Criteria: * Age \< 18 years. * Presence of comorbid conditions that may independently affect swallowing or voice functions. * Patients who withdraw consent or request to discontinue participation during or after the treatment period. * History of psychiatric disorders or use of psychiatric medications that may interfere with study participation or completion of patient-reported outcome measures.
Interventions
Quality of Life Assessment
OTHER
Patient Satisfaction Assessment
OTHER
Swallowing Function Assessment
OTHER
Voice Assessment
OTHER
Pain Assessment
OTHER
Anxiety and Depression Assessment
OTHER
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
02.04.2026
Completion date
31.12.2027
Registry ID
NCT07320820
Source
clinicaltrials.gov
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