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Connect Qualitative Interviews

Maximizing Communication of Evidence to Inform the Public to Engage in Observational Research for Cancer Prevention

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07444411
Enrollment
15
Registered
2026-03-02
Start date
2025-06-12
Completion date
2026-06-30
Last updated
2026-03-02

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

Conditions

Qualitative Research, Research Awareness

Brief summary

Goal of the study is to conduct Qualitative Interviews to identify and address barriers to study enrollment from various communities in order to increase the effectiveness and reach of our research to all people in the USA.

Detailed description

A major aim of study is to increase the impact of observational research studies and to improve information disseminated to the broader U.S. public by maximizing trust with researchers and providing clear evidence that can assist in making informed healthcare decisions, improving healthcare delivery, and improving outcomes. The study aims to garner public and patient input to inform best practices for engaging with patients, caregivers, and the broader healthcare community; identifying their research priorities; and reducing risk factors that lead to many non-communicable diseases including cancer.

Interventions

This is an exploratory qualitative study consisting of one semi-structured interview

OTHERQualitative Interview

Qualitative Interview with study participants

OTHERSurvey using a questionnaire.

This is an exploratory qualitative study consisting of one semi-structured interview

Sponsors

Baylor Research Institute
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients of Baylor Scott and White Health * Age between 30 and 70 years old at study invitation

Exclusion criteria

* Individuals with a history of invasive cancer (other than non-melanoma skin cancer) * Individuals with known cognitive impairment documented in their medical record

Design outcomes

Primary

MeasureTime frameDescription
Qualitative InterviewsFrom enrollment to the end of the study at 6 monthsConduct Qualitative with the Connect Study participants to identify and address barriers to enrollment from various communities in order to increase the effectiveness and reach of our research to all people in the USA.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKatherine Sanchez, PhD

Baylor Scott and White Research Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026