About this trial
This study is aiming to look into patients' treatment preferences and their socio economic background as well as the exploration of thought processes leading to these preferences. It will integrate, in two exploratory questionnaires, the three most common treatment schema (standard of care, non-operative management, surgery alone) all of which have been demonstrated efficacious.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
New rectal cancer patient
Operable patients
Capable adults older than 18 years of age
Capacity to sign a consent form
Disqualifiers
Patient unable to sign a consent form
Patients with metastasis
Recurrent tumours
Inability to answer questionnaires on an online platform
Trial population
This study will evaluate 192 participants: * 14 physicians (group A) * 178 patients (group B)
Trial design
Case-control
Other
Treatments tested in this trial
The only intervention will be the information brochure that will be given after the first questionnaire.
BehavioralThe information brochure will be given to both groups at the same time at 2-3 weeks after the first consultation (patients group) or after answering the first questionnaire (physicians group).
Treatment groups
Trial outcomes
Primary outcomes
Socio-economic and demographic characteristics
The primary study objective is to evaluate socioeconomic and demographic factors involved in patients' / physicians treatment preferences. This will be evaluated with the first questionnaire given at the time of the first consultation or when first approached by a research team member.
Secondary outcomes
Tradeoff level
The second objective is to assess the tradeoff level between the benefits versus quality of life. This will be evaluated with the second questionnaire given 2-3 weeks after the first consultation or after answering the first questionnaire.
Sponsors and contacts
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