MD Anderson Cancer Center
Houston, Texas, 77030, United States
NCT Number: NCT07674797
To examine how we can provide supportive care for patients with advanced cancer better tailored to their needs
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Houston, Texas, 77030, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Eligibility Criteria
Exclusion criteria
. Cognitive impairment in the opinion of the oncologist necessitating need for a surrogate decision making.
Patient will complete questionnaires and physical exams
Time frame: Through study completion; an average of 1 year
Contact information is provided by the study sponsor or research team.
M.D. Anderson Cancer Center
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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