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Recruiting NCT07756515

NCT07756515 Chatbot Implementation In The Clinical Informed Consent Process

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Clinical Trial Summary
NCT ID NCT07756515
Status Recruiting
Phase —
Sponsor M.D. Anderson Cancer Center
Condition Informed Consent
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2026-09-11
Primary Completion 2028-12-17

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
CoCo Chatbot

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2026-09-11 with a primary completion date of 2028-12-17.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to determine the feasibility of implementing the chatbot "CoCo" in the IC process for research studies. We hypothesize that implementing a chatbot into the IC process will facilitate accurate information delivery and enhance participant comprehension and process satisfaction compared to traditional remote consent methods.

Eligibility Criteria

Inclusion Criteria: * Ability to understand and willingness to provide informed consent. * Age ≥18 years. * Patients whose preferred language is English. * Patients who are being considered for enrollment in selected clinical research studies. Phase I will be initiated using the Clearinghouse protocol PA11-0852, a non-interventional biomarker study. Exclusion Criteria: N/A

Contact & Investigator

Central Contact

Funda Meric-Bernstam, MD

✉ fmeric@mdanderson.org

📞 (713) 794-1226

Principal Investigator

Funda Meric-Bernstam, MD

PRINCIPAL INVESTIGATOR

UT MD Anderson

Frequently Asked Questions

Who can join the NCT07756515 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Informed Consent. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07756515 currently recruiting?

Yes, NCT07756515 is actively recruiting participants. Contact the research team at fmeric@mdanderson.org for enrollment information.

Where is the NCT07756515 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT07756515 clinical trial?

NCT07756515 is sponsored by M.D. Anderson Cancer Center. The principal investigator is Funda Meric-Bernstam, MD at UT MD Anderson. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology