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Developing a screening for distress during cancer– A prospective longitudinal study of patients with oral cancer.

Recruiting
Conditions
C44
Other malignant neoplasms of skin
Registration Number
DRKS00008921
Lead Sponsor
Medizinische Hochschule Hannover, Klinik und Gesichtschirurgie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

squamous cell carcinoma

majority

Written informed consent

Exclusion Criteria

No possibility for follow-up survey,

drug addiction,

mental disability,
need of a carer

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patients will be asked about their personality , personal resources, their distress level and demographic data prior to biopsy ( T1 ) , after their surgery ( T2 ) 3months after ( T3 ) , six months thereafter, and 9 months are surveyed after terms They shall fill out a newly developed screening and the Distress Thermometer .The aim is to vailidate the new screening
Secondary Outcome Measures
NameTimeMethod
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