Patient explicit consideration of tradeoffs in decision making about rectal cancer treatment: benefits for decision process and quality of life.
Arwen H Pieterse, Marleen Kunneman, Wilbert B van den Hout...
https://pubmed.ncbi.nlm.nih.gov/30971150Actively Recruiting
Led by Sir Mortimer B. Davis - Jewish General Hospital · Updated on 2026-05-14
192
Participants Needed
1
Research Sites
4 weeks
Total Duration
Researchers are investigating how patients with operable rectal cancer and physicians make decisions about treatment options, focusing on their treatment preferences and socioeconomic and demographic backgrounds. The study also explores the balance between treatment benefits and quality of life. This observational study involves 192 participants, including 178 patients and 14 healthcare professionals, to better understand the thought processes behind treatment choices. Participants will complete two electronic questionnaires. The first gathers socio-demographic data, clinical information, and current knowledge about treatments. After this, all participants receive an informational brochure describing common treatment options, such as standard care, non-operative management, and surgery, including details about treatment length, potential side effects, and cancer outcomes. The second questionnaire assesses participants' treatment preferences and the tradeoffs they consider between benefits and quality of life. Participants are approached at clinical visits or through the research team and provide electronic consent before participation. All study materials, including consent forms, brochures, and questionnaires, are delivered electronically. The primary outcome measures include socio-economic and demographic characteristics, while secondary measures focus on the level of tradeoff participants make between treatment benefits and quality of life. The study is expected to conclude by January 2028.
CONDITIONS
Tradeoffs in Patient Decision Making About Rectal Cancer Treatment: Benefits Compared to Quality Of Life.
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) for eligibility assessment
Duration - 2 to 3 weeks
Participants who consent complete initial questionnaires about socio-demographic and clinical data, then receive an informational brochure about treatment options.
Questionnaires and brochure provided electronically; no in-person visits required
Duration - 1 day
Participants complete a second questionnaire evaluating their treatment preferences and tradeoff between benefits and quality of life.
1 electronic questionnaire completion
Total: 1 location
1
Jewish General Hospital
Montreal, Quebec, Canada, H3T 1E2
Actively Recruiting
E
Emma Starr, BHSc
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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