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NCT Number: NCT07390435

Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials

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.

Recruiting

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Key information

Conditions

Cancer Neoplasms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

BCCA - Kelowna, Kelowna, British Columbia, Canada

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Social Determinants of Health Questionnaire

Other

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

Primary outcomes

  1. 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 trial

    Time frame: 12 months

Secondary outcomes

  1. To assess the acceptability of this SDoH questionnaire to participants.

    Time frame: 12 months

Study contacts

Contact information is provided by the study sponsor or research team.

Anna Johnson

CONTACT

[email protected]

613-533-6430

Mariam Jafri

CONTACT

[email protected]

613-533-6430

Sponsors and collaborators

Lead sponsor

Canadian Cancer Trials Group

Network

Registry information

Acronym: FACTOR

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 5, 2026
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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