Pathos: Tradeoffs in Patient Decision Making About Rectal Cancer Treatment: Benefits Compared to Quality Of Life.

Sponsor
Sir Mortimer B. Davis - Jewish General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04925154
Collaborator
(none)
28
1
5.6
5

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: The only intervention will be the information brochure that will be given after the first questionnaire.

Detailed Description

The primary study objective is to evaluate socioeconomic and demographic factors involved in patients' / physicians treatment preferences. The secondary objective is to assess the tradeoff level between the benefits versus quality of life.

This study will evaluate 28 participants: 14 physicians (group A) and 14 patients (group B).

Participants with operable rectal cancer or health professionals will be screened for eligibility. Subsequently, these participants will be offered to participate in this pilot study and provided a consent form. When a participant has consented to participate, he/she will be provided with a first questionnaire (socio-demographic characteristics, some clinical data and medical baseline information as well as details about their current knowledge about treatments).

An informational brochure will be given after answering the first questionnaire describing different treatment regimens, treatment duration, potential side effects and oncologic outcomes.

A second questionnaire will be provided (evaluating patients treatment preferences and tradeoff).

The consent form, brochure and questionnaires will be available only in an electronic format (Microsoft Form).

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
28 participants
Observational Model:
Case-Control
Time Perspective:
Other
Official Title:
PILOT STUDY: PATHOS Tradeoffs in Patient Decision Making About Rectal Cancer Treatment: Benefits Compared to Quality Of Life.
Actual Study Start Date :
Dec 13, 2021
Anticipated Primary Completion Date :
May 1, 2022
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Group A: Patients

Recruitment for this group will take place at either the radiation-oncology department or at the colorectal surgery department, at the time of consultation or at the time of diagnosis, before the treatment setting. Once clinical staging is available, the surgeon and/or radiation-oncologist and/or research assistant should identify eligible patients. Patients that comply with selection criteria (inclusion/exclusion) will be approached by a research team member. For those patients interested in participating, the e-link to the consent form for this group will be sent by email. Once a patient decides to sign the consent form, the link for the questionnaire Q1 will be sent by email.

Behavioral: The only intervention will be the information brochure that will be given after the first questionnaire.
The 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).

Group B: Physicians

Health professionals will be approached by the research team. The study aim will be explained, and participants that agree to participate will be provided an e-link to consent for this group. Once the health care participant decides to sign the consent form, the link for the questionnaire Q1 will be sent by email.

Behavioral: The only intervention will be the information brochure that will be given after the first questionnaire.
The 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).

Outcome Measures

Primary Outcome Measures

  1. Socio-economic and demographic characteristics [1 day]

    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 Outcome Measures

  1. Tradeoff level [1 day]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Group A

  • New rectal cancer patient

  • Operable patients

  • Capable adults older than 18 years of age

  • Capacity to sign a consent form

  • Capacity to answer questionnaires on an online platform Group B

  • Treating physician specialists

  • Capacity to sign a consent form

  • Capacity to answer questionnaires on an online platform

Exclusion Criteria:
Group A:
  • Patient unable to sign a consent form

  • Patients with metastasis

  • Recurrent tumours

  • Inability to answer questionnaires on an online platform

  • Inability to communicate in french or english

Group B:
  • Participant unable to sign a consent form

  • Inability to answer questionnaires on an online platform

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jewish General Hospital Montreal Quebec Canada H3T 1E2

Sponsors and Collaborators

  • Sir Mortimer B. Davis - Jewish General Hospital

Investigators

  • Principal Investigator: Té Vuong, Lady Davis Institute - JGH

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Te Vuong, Radiation-oncologist, Sir Mortimer B. Davis - Jewish General Hospital
ClinicalTrials.gov Identifier:
NCT04925154
Other Study ID Numbers:
  • 2021-2517
First Posted:
Jun 14, 2021
Last Update Posted:
Dec 29, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Te Vuong, Radiation-oncologist, Sir Mortimer B. Davis - Jewish General Hospital

Study Results

No Results Posted as of Dec 29, 2021