Quality of Life and Psychological Well-being in Patients With Malignant Melanoma

Sponsor
University Hospital Freiburg (Other)
Overall Status
Unknown status
CT.gov ID
NCT00963261
Collaborator
Essex Pharma GmbH (Industry), Universitätsklinikum Köln (Other)
600
2
2
36
300
8.3

Study Details

Study Description

Brief Summary

The purpose of this study is to analyse the physical and psychological side-effects in the course of treatment with IFN-alpha. The effectiveness of a specific intervention for the management of these side-effects is evaluated.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: psycho-oncological intervention
N/A

Detailed Description

Today, the consideration of the side effects of intensive treatment measures and their influence on quality of life are regarded as standard procedures in oncology. Quality of life measurements have found their way into clinical studies as patient-reported outcomes. In comparison to other tumor types, the field of dermato-oncology has had less research activity concerning quality of life. However, in recent years more attention has been paid to health related quality of life in malignant melanoma patients, especially under adjuvant treatment with interferon-alpha. Data about high dose IFN-α treatment, especially from the USA, show that there are significant physical and psychological side effects, such as fatigue and depression, which often lead to dosage reduction or termination of treatment. As yet, there are very few systematic studies about low dose IFN-α treatment, especially in regard to the side effects during the course of the disease.

Concerning treatment side-effects it is known throughout various areas of oncology that specific psycho-oncological interventions assist in the patients' adaptation to the illness and handling of the side effects of therapy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
600 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Side-effect Management for Patients With Malignant Melanoma Undergoing Treatment With Interferon Alpha (IFN-α)- Diagnosis and Therapy -
Study Start Date :
Apr 1, 2009
Anticipated Primary Completion Date :
Feb 1, 2011
Anticipated Study Completion Date :
Apr 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: psycho-oncological intervention

stepped care psycho-oncological intervention

Behavioral: psycho-oncological intervention
stepped care treatment program with different elements (patient information, exercise, psychoeducation, individual and group therapy, psycho-pharmacology)

No Intervention: control group

Outcome Measures

Primary Outcome Measures

  1. Changes in quality of life [1 year]

Secondary Outcome Measures

  1. Changes in fatigue [1 year]

  2. Changes in psychological distress [1 year]

  3. Changes in depressive syndrome [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Documented and proven stage Ib up to stage IIIc malignant melanoma

  • No clinical and radiological evidence or suspicion of persistent disease

  • Treatment with IFN-α within a study or analog treatment schedule with IFN-α

  • ECOG performance status < 2

  • Constant after care

  • Informed consent to participate in the study

  • melanoma diagnosis within the last 5 years or therapy, recurrence or progression within this period of time.

Exclusion Criteria:
  • Inoperable lymph nodes- or distant metastases

  • Tumors of other origins or localisations within the past 10 years

  • Severe and permanent infectious diseases, e. g. HIV or hepatitis

  • Participation in other treatment studies apart from IFN-α

  • Insufficient knowledge of German language

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Medical Center Freiburg, Department of Dermatology Freiburg Germany 79104
2 University Medical Center Collogne, Department of Dermatology Köln Germany 50937

Sponsors and Collaborators

  • University Hospital Freiburg
  • Essex Pharma GmbH
  • Universitätsklinikum Köln

Investigators

  • Principal Investigator: Katrin Reuter, PhD, University Medical Center Freiburg, Department of Psychiatry and Psychotherapy
  • Principal Investigator: Dorothee Nashan, MD, University Medical Center, Department of Dermatology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00963261
Other Study ID Numbers:
  • PO5098
First Posted:
Aug 21, 2009
Last Update Posted:
Jun 25, 2010
Last Verified:
Jun 1, 2010
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 25, 2010