Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials

ConditionCancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCanadian Cancer Trials Group

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Currently being screened and consented to a CCTG trial (prospective).

Already enrolled in an ongoing CCTG trial and still under follow-up (retrospective).

Disqualifiers

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

Trial population

This study is designed to include participants who have consented to a CCTG clinical trial. If a patient consents to a CCTG trial but does not enroll, they will remain eligible for SC.32S.

Trial design

Design model

Ecologic or community

Time perspective

Other

Treatments tested in this trial

  • Social Determinants of Health Questionnaire

    Other intervention

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

Treatment groups

No treatment groups listed

Trial outcomes

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

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.