patients with squamosa cell cancer of the mouth
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Histologically confirmed squamous cell carcinoma of the oral cavity (OSCC). Capacity to provide informed consent: Participants must possess the cognitive ability to understand the nature, significance, and implications of the study. Voluntary participation: Submission of a signed written informed consent form, provided without coercion and with the understanding that withdrawal is possible at any time
Exclusion criteria
Exclusion criteria: Inability to undergo examination due to poor performance status Pre-existing psychiatric disorders diagnosed prior to the initial oncological diagnosis: Pre-existing major depressive disorder (severe). Schizoaffective disorder Bipolar affective disorder. Schizophrenia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) self efficacy (Schwarzen and Jerusalem 1995) 1 day preoperatively, 10 days postoperatively, 3 month postoperatively, 6 month postoperatively 2)Quality of life in head and neck cancer patients (EORTC QLQ-H&N35) 1 day preoperatively, 10 days postoperatively, 3 month postoperatively, 6 month postoperatively 3) Health-related Quality of life (SFQ12) 1 day preoperatively, 10 days postoperatively, 3 month postoperatively, 6 month postoperatively 4) Distress Questionnaire (DKG) 1 day preoperatively, 10 days postoperatively, 3 month postoperatively, 6 month postoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| Pictorial Representation of Illness and Self-Measure (PRISM), Oral Health-Related Quality of Life (OHIP-G5), Short Form of the Social Support Questionnaire (F-SozU-K14), therapeutic Alliance (WAI-Tu), progression-free survival 1 day preoperatively, 10 days postoperatively, 3 month postoperatively, 6 month postoperatively | — |
Countries
Germany
Contacts
Universitätsklinikum Leipzig - Abteilung für Mund-, Kiefer- und Gesichtchirurgie