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Clinical Trial Summary

This trial studies the attitudes and beliefs of high risk patients and caregivers regarding the prescription of intranasal naloxone spray for opioid overdose. Knowledge regarding high risk patients' and caregivers' beliefs and attitudes regarding co-prescription of naloxone spray with opioids may help to identify barriers to prescribing and helping tailor the education to better meet the needs of patients and caregivers.


Clinical Trial Description

PRIMARY OBJECTIVE: I. To determine the proportion of high risk patients who perceive receiving a prescription of intranasal naloxone to be beneficial for them. SECONDARY OBJECTIVES: I. To determine the proportion of caregivers who perceive receiving a prescription of intranasal naloxone to be beneficial for the patient. II. To determine the association between high risk patients' and their caregivers' characteristics (this includes cut-annoyed-guilty-eye [CAGE], screener and opioid assessment for patients with pain [SOAPP], age, gender, ethnicity, education, employment status, presence of caregiver, cancer type, cancer stage, reason for Narcan prescription, health insurance, and setting of Narcan prescription) and their perception that a prescription for intranasal naloxone is beneficial for patients. EXPLORATORY OBJECTIVE: I. To conduct an exploratory analysis of high risk patients' and caregivers' attitudes and beliefs regarding prescription of intranasal naloxone spray. OUTLINE: Participants complete a survey over 30 minutes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04129138
Study type Observational
Source M.D. Anderson Cancer Center
Contact Jaya S. Amaram-Davila, MD
Phone (713) 792-6085
Email jsamaram@mdanderson.org
Status Recruiting
Phase
Start date July 18, 2020
Completion date June 30, 2024

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