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RecruitingNCT06036810Updated Oct 7, 2026

Spanish Decision Tool for Ovarian Cancer Maintenance Therapy

An interventional study of Shared Medical Decision Tool and Engaging Patients in Decision Making in Ovarian Cancer, sponsored by M.D. Anderson Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-07.

Sponsored by M.D. Anderson Cancer Center · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Started Aug 2023; still recruiting 3 years 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

To develop a shared decision-making (SDM) tool to help Spanish-speaking patients make decisions about their maintenance therapy

Read the detailed description

Objectives:

  • Create a low literacy version of a shared decision-making (SDM) tool for ovarian cancer maintenance therapy for Spanish speaking individuals.
  • To explore the feasibility and acceptability of incorporating the SDM tool into routine clinical care for Spanish speaking individuals.
  • To estimate the effectiveness of the SDM tool on quality of the decision making in patients with ovarian cancer who are making decisions about maintenance therapy through a pilot study.
02

Conditions studied

  • Ovarian Cancer

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03

In context

Ovarian Neoplasms

2,695 studies on the registry are indexed under Ovarian Neoplasms; 726 are open to participants now.

This study's planned enrollment of 70 is above the median of 60 across 2,030 interventional studies indexed under Ovarian Neoplasms.

Browse Ovarian Neoplasms studies →

Lead sponsor

M.D. Anderson Cancer Center is the lead sponsor of 2,999 studies on the registry; 579 are open to participants now.

Of its 599 completed or terminated interventional studies of FDA-regulated products, 402 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Study population: This study will enroll patients and clinical providers.

Inclusion criteria: Patients

  • Eligible patients must be: 1) individuals ≥ 18 years with advanced stage high grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are receiving or have completed platinum-based chemotherapy for ovarian cancer and are potentially eligible to receive maintenance therapy; 2) able to understand, speak or read in Spanish.

Exclusion criteria: Patients

  • Inability or unwillingness to sign informed consent

Inclusion criteria: Clinicians

  • Eligible clinicians will include: 1) MD Anderson gynecologic oncologists and advanced practice providers who practice at the Houston Area Locations (HALs), MD Anderson Cancer Center, or our county safety net hospital, The Harris Health System (LBJ Hospital).

Exclusion criteria: Clinicians

  • Inability or unwillingness to sign informed consent
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Study Phase 1

    Pre-testing and cognitive interviews for the Decision Support Tool

    Other: Shared Medical Decision Tool · Behavioral: Engaging Patients in Decision Making · Behavioral: Literacy Spanish Language

  • Experimental
    Study Phase 2

    Usual Care (Control Group) or Participants utilize the Decision Support Tool with Provider guidance (Intervention Group).

    Other: Shared Medical Decision Tool · Behavioral: Engaging Patients in Decision Making · Behavioral: Literacy Spanish Language

Interventions

  • OtherShared Medical Decision Tool

    standard of care

  • BehavioralEngaging Patients in Decision Making

    standard of care

  • BehavioralLiteracy Spanish Language

    standard of care

06

What researchers measure

Primary outcomes

  1. Decision Regret Scale questionnaire

    This scale measures decisional regret related to health care decisions at a specific point in time. This tool consists of 5 questions answered on a Likert scale (1="Strongly agree" to 5="Strongly disagree").

    Time frame: through study completion; an average of 2 year.

07

Study locations

1 of 1 sites recruiting
  • M D Anderson Cancer Center
    Houston, Texas 77030, United States
    • Larissa Meyer, M D · Contact · lmeyer@mdanderson.org · 713-745-0973
    • Larissa Meyer, MD · Principal investigator
    Recruiting
08

References and documents

09

Updates

1 registry update since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
1 update, last Oct 7, 2026
Show all 1 update
  1. Oct 7, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06036810
Lead sponsor
M.D. Anderson Cancer Center
Responsible party
Sponsor
First posted
Sep 14, 2023
Start date
Aug 31, 2023
Primary completion
Oct 31, 2027 (estimated)
Completion
Oct 31, 2027 (estimated)
Last update
Oct 7, 2026

Study contacts

Larissa Meyer, M D
Contact
Lmeyer@mdanderson.org
(713) 745-0973
Larissa Meyer, Meyer
principal investigator · M.D. Anderson Cancer Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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