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Psychological Distress in Outpatient Oncological Rehabilitation

NCT04324320 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 165

Last updated 2020-03-27

No results posted yet for this study

Summary

The aim of the study is to assess psychological distress and co-morbidity as well as relevant sociodemographic, anthropometric, medical and functional data in patients treated at the Outpatient Clinic for Oncological Rehabilitation at the Department of Physical Medicine, Rehabilitation and Occupational Medicine at the Medical University of Vienna.

Conditions

Interventions

DIAGNOSTIC_TEST

medical assessment

medical assessment includes the collection of * sociodemographic data * anthropometric data (weight, height, body mass index) * medical data * psycho-oncologic basis assessment (PO-BADO questionnaire) * pain assessment (VAS: visual analogue scale) * 3 functional tests: * handgrip strength * 6 Minute Walking Test * Timed Get up and Go Test

DIAGNOSTIC_TEST

psychological assessment

psychological assessment includes several standardized screening and assessment questionnaires and tools: * quality of life: SF-36 * anxiety, depression, stress: Hospital Anxiety and Depression Scale (HADS-D) * subjective stress perception: Perceived Stress Scale (PSS-10) * resilience: resilience scale (RS-13) * fatigue: Brief Fatigue Inventory (BFI) * disability related to pain: Pain Disability Index (PDI) * workability: Work Ability Index - short version (WAI-K) * psychological assessment based on the checklist of the International Diagnoses (IDCL) for ICD-10 and the ICD-10 checklist of symptoms for psychological disorders (SCL))

Sponsors & Collaborators

  • Medical University of Vienna

    lead OTHER

Principal Investigators

  • Richard Crevenna, Prof MD MBA MMSc · Medical University of Vienna

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-30
Primary Completion
2021-12-31
Completion
2022-12-31

Countries

  • Austria

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04324320 on ClinicalTrials.gov