Improving Comprehensive Care for Cancer Patients

This study is testing an intervention called OPTIMISE to help cancer patients better manage their health conditions and improve communication between their cancer doctors (oncologists) and primary care doctors. You may be able to join if you are an adult (18 years or older) recently diagnosed with early-stage breast, gastrointestinal (GI), or hematologic (blood) cancer, and are also managing other chronic health conditions like diabetes or high blood pressure. The study wants to see if OPTIMISE helps you feel more involved in your own care and improves how you manage your health, measured at 4 months after you start treatment. The study is currently recruiting 340 participants, but its overall status is unclear.

Study design
This is a randomized controlled trial involving 300 medically underserved patients with breast, GI, or hematological cancer and other health conditions. Participants will be split into two groups: one receiving usual medical care and the other receiving the OPTIMISE intervention.
What's involved
You will complete surveys at the start of your cancer treatment, at 2 and 4 months after treatment begins, when you receive your Survivorship Care Plan (SCP), and then at 3, 6, and 12 months after receiving your SCP.
Compensation
Not stated in the trial record.
Follow-up
You will be followed for at least 12 months after receiving your Survivorship Care Plan (SCP) to complete surveys.

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NCT05323409

Improving Comprehensive Care of Cancer Patients

Recruiting
NAAges 18+InterventionalSupportive care
Baylor College of Medicine
~340 participants
Updated 2026-06-30 on ClinicalTrials.gov
What's tested:OPTIMISE

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Patient Activation Measure (PAM)
Measured over 4 month follow-up
+1 more outcome measured
Breast Cancer
Gastrointestinal Cancer
Hematologic Cancer
1 sites across 1 states
Texas1
  • Hoda Badr · PRINCIPAL_INVESTIGATOR · Baylor College of Medicine

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

For patients: 1) new diagnosis or within three months of treatment initiation for early-stage breast (I-IIIB), GI (Stage I-III), or hematologic (Stage I-III) cancer 2) treatment with standard, definitive therapies (may include one or more modalities) 3) presence of one or more chronic comorbidities (e.g., diabetes, hypertension) and/or unhealthy lifestyle behaviors (e.g., overweight/obesity, current smoker, alcohol use) that require ongoing management during cancer treatment 4) age \>18 years 5) fluency in English or Spanish 6) ability to provide informed consent 7) assignment to a Harris Health oncologist and PCP who are willing to participate and will provide informed consent.

Exclusion

For Patients: Significant cognitive impairment or Lack of capacity to consent For Providers: None
  • Patient Activation Measure (PAM)4 month follow-up

    self-management attitudes

  • Instrument to measure Self-Management (IMSM)4 month follow-up

    self-management behaviors