ID
Bron
Verkorte titel
Aandoening
colorectal cancer, average risk individuals
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
- Attendance rate
Achtergrond van het onderzoek
Colorectal cancer (CRC) is one of the major causes of death in the Netherlands, accounting for over 4500 deaths in 2005. CRC morbidity and mortality can be reduced by population screening. Of the
currently available screening tests, the effectiveness of screening with fecal occult blood test (FOBT) is
the only one with documented efficacy in randomized controlled clinical trials.
FOBT is a test with a relatively low sensitivity. On the other hand, it is not invasive and very cheap.
Biannual performance of FOBT could result in a cumulative yield that is competitive with the yield of
screening with more sensitive tests performed less frequently. Most international guidelines on
FOBT-based screening now recommend biannual screening.
The benefits of a screening program depend not only on the efficacy, but also on the participation rate.
Biannual screening is only feasible if the participation rate in such a screening program does not
substantially decline during subsequent screening rounds.
So far, it is unclear to what extent screening participants respond positively to invitations for repeated
screening in the Dutch situation and how many of them actually will participate in further screening
rounds. Preliminary analysis of questionnaires from the first screening round of the Dutch FOBT
implementation trial suggests that a significant percentage of the participants would not participate again
in an FOBT-based screening program.
In this proposal we intend to study the implementation of repeated FOBT in participants of
invitation-based FOBT population screening in the Netherlands. The study will build on the first
implementation study of FOBT screening in the Amsterdam region which has almost been completed.
Eligible for the current study proposal will be the same 10.000 persons aged 50 to 74 years that were
selected for the first screening round in the above mentioned implementation study. This group will
consist of non participants of the first round as well as those that tested negative on the FOBT test.
Those people that were FOBT-positive but declined undergoing a colonoscopy will also be included in
the second round. Only FOBT-positives that underwent a colonoscopy will be excluded since they have
undergone the current gold standard of colon imaging. The above mentioned group (± 9.750 persons)
will receive another invitation to participate in FOBT screening two years after the first invitation. In this
study we intend to use the immunochemical FOBT (OC-Sensor). In case of a positive FOBT they will be
referred for colonoscopy. The main outcome measure of this study is the second round participation
rate.
Validated questionnaires, provided before and after test results, will measure patients' experience with
the screening program. Most important aspects are the perception of the repeated FOBT, the
understanding of the test results, the possibility to make a well-informed choice, and the preference of
screening method. Furthermore, we will incorporate the results of this two-yearly FOBT-based
population screening program in a model-based cost-effectiveness analysis of CRC-screening in the
Netherlands.
The organization of the study will be done by the Departments of Gastroenterology and Hepatology and
Clinical Epidemiology, Biostatistics and Bioinformatics in the AMC, together with the regional
Comprehensive Cancer Center (IKA). The cost-effectiveness analysis will be performed in collaboration
with the department of Public Health of the Erasmus MC.
The results of this implementation study will enable an evidence-based comparison of the different
FOBT-strategies for CRC-screening in the Netherlands from a point of feasibility and cost-effectiveness.
Onderzoeksopzet
- Baseline (after completion of the test, before notification of the testresult)
Onderzoeksproduct en/of interventie
FOBT with collection paper vs FOBT without collection paper
Algemeen / deelnemers
Department of Gastroenterology
C2-231
M.J. Denters
Meibergdreef 9
Amsterdam 1105 AZ
The Netherlands
+31 (0)20 5666464 / +31 (0)20 5669111 sein 63500
m.j.denters@amc.uva.nl
Wetenschappers
Department of Gastroenterology
C2-231
M.J. Denters
Meibergdreef 9
Amsterdam 1105 AZ
The Netherlands
+31 (0)20 5666464 / +31 (0)20 5669111 sein 63500
m.j.denters@amc.uva.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Age 50-74
2. Living in Almere, Amsterdam
3. Watergraafsmeer, Diemen
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. FOBT positive in first round
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL1281 |
NTR-old | NTR1327 |
Ander register | : 120710007 |
ISRCTN | ISRCTN wordt niet meer aangevraagd |