Recruiting

Observational Study

Sponsor:

M.D. Anderson Cancer Center

Code:

NCT07382557

Conditions

Lung Cancer

Eligibility Criteria

Sex: All

Age: 50 - 70+

Healthy Volunteers: Accepted

Interventions

Surveys

Focus groups

Cognitive Interviews

Lung cancer screening decision aid video

Colon cancer screening video

Study Details

Brief summary:

The goal of the study is to adapt and test a participant decision aid about lung cancer screening for use with patients in theHarris Health System (HHS).

Conditions

Lung Cancer

Study ID

NCT07382557

Start date

Sep 29, 2022

Status verified date

Jan, 2026

Completion date

Feb 2, 2027

Anticipated

Primary completion date

Feb 2, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 50 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

1. 50-80 years of age
2. Current smokers or smokers who have quit less than 15 years ago
3. Speak either English or Spanish
4. No history of lung cancer
5. Family member of someone with a history of smoking AND lung cancer

Exclusion Criteria:

Study Design

Enrollment

360 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Other

Interventions and Outcome Measures

Arms

other: Needs Assessment: Provider Survey (Aim 1)

Up to 200 physicians and other health professionals

other: Needs Assessment: Patient/Family member Focus Groups (Aim 1)

Up to 20 participants who speak English or Spanish

other: Decision Aid Adaptation (Patient Cognitive Interviews (Aim 1)

Up to 40 participants who speak English or Spanish

experimental: Pilot Study: Intervention Patients (Aim 2)

Up to 50 participants (25 English speakers, 25 Spanish speakers)

placebo comparator: Pilot Study: Control Patients (Aim 2)

Up to 50 participants (25 English speakers, 25 Spanish speakers)

Interventions

Surveys

Investigators will answer surveys about their lung cancer screening practices

Focus groups

Participants will participate in focus groups about information they need in order to decide about lung cancer screening

Cognitive Interviews

Participants will participate in interviews about their understanding of the adapted video script

Lung cancer screening decision aid video

Participants take surveys before and after watching the intervention video

Colon cancer screening video

Participants take surveys before and after watching the control video

Primary outcome measure

  • Safety and Adverse Events (AEs). [ Time Frame: Through study completion; an average of 1 year ]

Central Contacts and Locations

Central contacts

Robert Volk, PHD

(713) 563-2509bvolk@mdanderson.org

Locations

The University of Texas M. D. Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Robert Volk, PHD

713-563-2509bvolk@mdanderson.org

Principal Investigator:

Robert Volk, PHD

More Information

Sponsor

M.D. Anderson Cancer Center

Last update posted

Feb 3, 2026

Last verified

Jan, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by M.D. Anderson Cancer Center on 2026-02-03.