Research AwarenessNCT07444411
Connect Qualitative Interviews
An observational study of Research Awareness and Qualitative Research, run by Baylor Research Institute at 1 site in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 30 to 70 yearsHealthy volunteers can take part
- Conditions the study is for
- Research Awareness, Qualitative Research
- What is being tested?
- Qualitative Interview, Qualitative Survey and Survey using a questionnaire.
- How many people
- 15 participants
- Where
- 1 siteUnited States
- Study dates
- 12 Jun 2025to 30 Jun 2026
- How long will I take part?
- 1 Year
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 to 70 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: BSW patients between the age of 30-70 with no history of cancer*
Who may be able to join
- Patients of Baylor Scott and White Health
- Age between 30 and 70 years old at study invitation
Who cannot join
- Individuals with a history of invasive cancer (other than non-melanoma skin cancer)
- Individuals with known cognitive impairment documented in their medical record
Trial locations and contacts
1 site in 1 country.
United States1 site
Baylor Scott and White Research Institute
Dallas, Texas, 75204
About this study
Official title: Maximizing Communication of Evidence to Inform the Public to Engage in Observational Research for Cancer Prevention
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.
Read the 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.
- Conditions
- Research Awareness, Qualitative Research
- Being tested
- Qualitative Interview, Qualitative Survey, Survey using a questionnaire.
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Qualitative InterviewOther
Qualitative Interview with study participants
Qualitative SurveyOther
This is an exploratory qualitative study consisting of one semi-structured interview
Survey using a questionnaire.Other
This is an exploratory qualitative study consisting of one semi-structured interview
| Study group | Role | What they receive |
|---|---|---|
| Connect Participants | Participants enrolled in the Connect for Cancer Prevention Study at BSWH Receives: Other: Qualitative Interview; Other: Qualitative Survey; Other: Survey using a questionnaire. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Qualitative Interviews
Conduct 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.
Measured: From enrollment to the end of the study at 6 months
Qualitative Interviews
Conduct qualitative interviews to understand barriers to enrollment from various communities in order to increase the effectiveness and reach of our research to all people in the USA.
Measured: From enrollment to the end of interviews at 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Mar 2026
- Study start12 Jun 2025
- Primary completion30 Jun 2026 (estimated)
- Study completion30 Jun 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Research AwarenessStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 15 participants (actual)
- Target duration
- 1 Year
Sponsor and investigators
- Lead sponsor
- Baylor Research Institute
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Responsible party
- Sponsor
- Investigators
- Katherine Sanchez, PhD, Principal investigator, Baylor Scott & White The Heart Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07444411
- Sponsor's protocol ID
- 025-308
- Status last verified
- Jun 2025
- First submitted
- 26 Feb 2026
- Last updated
- 2 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 2 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Maximizing Communication of Evidence to Inform the Public to Engage in Observational Research for Cancer Prevention
- ClinicalTrials.gov ID
- NCT07444411
- Acronym / sponsor ID
- 025-308
- Conditions
- Research Awareness, Qualitative Research
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 15 participants (actual)
- Lead sponsor
- Baylor Research InstituteUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Study start
- 12 Jun 2025 (actual)
- Primary completion
- 30 Jun 2026 (estimated)
- Study completion
- 30 Jun 2026 (estimated)
- First posted
- 2 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Target follow-up
- 1 Year
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Connect Participants | – | Other: Qualitative Interview, Other: Qualitative Survey, Other: Survey using a questionnaire.Participants enrolled in the Connect for Cancer Prevention Study at BSWH |
Who may qualify
- Ages
- 30 to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- BSW patients between the age of 30-70 with no history of cancer*
Key inclusion criteria (2 listed)
- Patients of Baylor Scott and White Health
- Age between 30 and 70 years old at study invitation
Key exclusion criteria (2 listed)
- Individuals with a history of invasive cancer (other than non-melanoma skin cancer)
- Individuals with known cognitive impairment documented in their medical record
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Qualitative InterviewQualitative Interview with study participants | Other | Connect Participants |
| Qualitative SurveyThis is an exploratory qualitative study consisting of one semi-structured interview | Other | Connect Participants |
| Survey using a questionnaire.This is an exploratory qualitative study consisting of one semi-structured interview | Other | Connect Participants |
Primary outcome
Qualitative Interviews
Time frame: From enrollment to the end of the study at 6 months
Conduct 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.
Qualitative Interviews
Time frame: From enrollment to the end of interviews at 6 months
Conduct qualitative interviews to understand barriers to enrollment from various communities in order to increase the effectiveness and reach of our research to all people in the USA.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Mar 2026.
- Individual participant dataSharing planned: Yes
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Katherine Sanchez, PhD principal investigator
Baylor Scott & White The Heart Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Research Awareness and Qualitative Research, run by Baylor Research Institute at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 2 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Qualitative Interviews (time frame: From enrollment to the end of the study at 6 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Mar 2026.