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Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials

Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07390435
Acronym
FACTOR
Enrollment
1000
Registered
2026-02-05
Start date
2026-05-15
Completion date
2027-06-30
Last updated
2026-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Brief summary

This study is being done to answer the following question: Are patients on a clinical trial willing to provide answers to questions about their social, economic, and environmental factors-sometimes called social determinants of health-which affect people's health experiences and access to care. These factors may include income, education, employment, housing, social supports, and experiences with discrimination or stress. Participation will help researchers better understand barriers to participating in clinical trials and access to health care.

Detailed description

It is anticipated that 1000 people will take part in this study. Participation in this study will only take about 10 minutes or less. Participants who choose to take part in this study will be asked to fill out a form with questions in English or French about the non-medical factors that influence health. This includes asking about the conditions and places in which the participant lives, learns, works, and plays. Participants will also be asked how they feel about answering these questions. Researchers will use this information to better understand who participates in clinical trials.

Interventions

This study will use a standardized SDoH Questionnaire to collect the required sociodemographic data

Sponsors

Canadian Cancer Trials Group
Lead SponsorNETWORK

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults (≥18 years) who are either: * Currently being screened and consented to a CCTG trial (prospective). * Already enrolled in an ongoing CCTG trial and still under follow-up (retrospective).

Exclusion criteria

* Participants already enrolled or expected to enroll in a CCTG trial that is also collecting the SDoH Questionnaire.

Design outcomes

Primary

MeasureTime frame
To evaluate the feasibility of collecting comprehensive sociodemographic data via a standardized SDoH Questionnaire among participants being screened and consented to a CCTG trial and participants already enrolled in a CCTG trial12 months

Secondary

MeasureTime frame
To assess the acceptability of this SDoH questionnaire to participants.12 months

Countries

Canada

Contacts

CONTACTAnna Johnson
ajohnson@ctg.queensu.ca613-533-6430
CONTACTMariam Jafri
mjafri@ctg.queensu.ca613-533-6430
STUDY_CHAIRLeah Lambert

BCCA - Vancouver Cancer Centre, Vancouver, BC Canada

STUDY_CHAIRMichael McKenzie

BCCA - Vancouver Cancer Centre

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026