| Registry | NCT07674797 |
|---|---|
| Status | Not yet recruiting |
| Phase | Not applicable |
| Study type | Interventional; randomized, single group, masking: none, supportive care |
| Enrollment | 300 (Estimated) |
| Sponsor | M.D. Anderson Cancer Center (Other); collaborators: National Institutes of Health (NIH) |
| Conditions | Oncologic, Palliative Care, Remote Monitoring, Electronic Assessments, Telehealth |
| Interventions | Questionnaire and Physical Exam (Other) |
| Dates | start 2026-11-22 (estimated), primary completion 2032-06-30 (estimated), completion 2034-06-30 (estimated), first posted 2026-06-30, last updated 2026-06-30 |
| Locations | 1 site in United States |
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To examine how we can provide supportive care for patients with advanced cancer better tailored to their needs
Primary Objectives Objective 1: To compare the impact of timely SPC referral and enhanced usual care (i.e., selective referral) on the proportion of participants with an outpatient SPC consultation at (a) 12 weeks (primary outcome) and (b) 24 weeks post-initial screening.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Dose Dense Timely SPC | Experimental | Other: Questionnaire and Physical Exam | |
| Enhanced UC | Experimental | Other: Questionnaire and Physical Exam | |
| Stadard Timely SPC | Experimental | Other: Questionnaire and Physical Exam |
Sex: All, ages: 18 Years to any
Eligibility Criteria * Age ≥ 18 * Outpatients who are within 12 weeks of diagnosis of metastatic solid tumors and seen by one of the participating medical oncologists * Eastern Cooperative Oncology Group Performance Status 0.2 * Able to speak English or Spanish Exclusion Criteria: . Cognitive impairment in the opinion of the oncologist necessitating need for a surrogate decision making. • Previously seen by SPC team at UT MD Anderson
| Facility | City | Country | Status |
|---|---|---|---|
| MD Anderson Cancer Center | Houston, Texas | United States |