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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00008921

Enrollment

100

Registered

2017-09-06

Start date

2016-04-13

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C44

Interventions

Group 1: Patients with squamous cell carcinoma are asked about their personality , their personal resources and their current burdens and demographic data prior to biopsy ( T1 ) , after their surgery

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: squamous cell carcinoma majority Written informed consent

Exclusion criteria

Exclusion criteria: No possibility for follow-up survey, drug addiction, mental disability, need of a carer

Design outcomes

Primary

Measure	Time frame
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	—

Countries

Germany

Contacts

Public ContactMadiha Rana

Helmut-Schmidt-Universität, Universität der Bundeswehr

rana at hsu-hh.de+49-40-6541-2932

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026