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A prospective randomized trial for the evaluation of a theoretical...

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Title A prospective randomized trial for the evaluation of a theoretical follow-up schedule in cutaneous melanoma patients, the MELFO-study.
Period 02 / 2006 - 12 / 2013
Status Current
Dissertation Yes
Research number OND1338591
Data Supplier Projectleider

Abstract

Rationale
The follow-up in cutaneous melanoma patients is controversial. The suggested aims of for follow-up are detection of recurrences, detection of second primary melanomas, quality evaluation of surgical treatment, patient reassurance and reduction of anxiety. Several authors have proposed follow-up schedules, but despite these attempts, no national or international evidence-based consensus has been achieved in the past decades. Moreover, no true evidence for the value of follow-up exists. Due to the increasing prevalence of melanoma patients, a definite high efficiency in a more evidence-based follow-up regimen for melanoma patients is required.
Objectives
To determine the difference between patients in the so-called experimental follow-up schedule and the conventional follow-up schedule, in patients? well-being, expressed in health related quality of life, level of anxiety and satisfaction with the follow-up schedule and in the sufficiency to detect recurrences and second primary melanomas. We expect to find no significant difference in patients? well-being scores between both groups. If the experimental follow-up schedule proves not to reduce patients? well-being significantly, this schedule may be proposed as the new follow-up surveillance schedule for melanoma patients and could be further elaborated and implemented in future guidelines.
Outline
In the MELFO-study AJCC stage IB-IIC cutaneous melanoma patients will be randomized between the conventional follow-up schedule derived from Dutch national guidelines and an experimental follow-up schedule adjusted to disease stage, resulting in less scheduled follow-up visits. The final outcome of the study will be determined after a minimum of 5 years of follow-up surveillance. Patients? well being will be measured at 0, 6, 12, 24, 36 48 en 60 months after diagnosis and inclusion via a questionnaire. This questionnaire consists of the RAND-36, the Impact of Events Scale, the Cancer Worry Scale, the STAI-DY and self-designed questions on ?Follow-up satisfaction?. During follow-up the incidence and types of recurrence detected, the person detecting the recurrences as well as the exact way of detection will be recorded.

Related organisations

Secretariat Department of Surgery (RUG)
Collaboration Isala Clinics
Collaboration Medical Spectrum Twente

Other involved organisations

Integraal Kankercentrum Noord-Oost
Medisch Centrum Leeuwarden

Related people

Researcher Dr. A.B. Francken
Researcher Dr. J.E.H.M. Hoekstra-Weebers
Project leader Prof.dr. H.J. Hoekstra
Doctoral/PhD student Drs. M.J. Speijers

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