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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03665298
Other study ID # 18-00652
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date February 2019
Est. completion date November 2019

Study information

Verified date December 2019
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Mobile health interventions offer a longitudinal approach to reducing the burden of substance use disorders and may stem the rise of the opioid overdose epidemic. Smartphone applications are one of the most popular mobile phone features nationally, among patients in addiction treatment, and among criminal justice involved (CJI) patients enrolled in addiction treatment. This research conducted at Bellevue Hospital's inpatient detoxification program established attitudes and self-reported behaviors favorable to theoretical smartphone applications addressing opioid use, HIV, and HCV prevention and management strategies. This study aims to assess the feasibility and usability of a smartphone application to enhance access to sterile needles, naloxone overdose kits, and addiction treatment programs in New York City.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 2019
Est. primary completion date November 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Fluent in spoken and written English;

- Meets or has previously met DSM-5 criteria for current opioid use disorder, of at least moderate severity;

- Owns or has owned a smartphone

Exclusion Criteria:

- Any patient who does not meet the inclusion criteria as above, is clinically unstable per the unit admitting physicians, refuses to participate in the study, or is cognitively impaired.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Smartphone Application
App that helps patients find syringe exchange programs, safe way to dispose of needles, access to naloxone kits and access to free medical care and addiction treatment programs.

Locations

Country Name City State
United States New York University School of Medicine New York New York

Sponsors (1)

Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility of Needle-X application number of patients enrolled, as this study will include a single interaction, at which point the patient will no longer be part of the study. 12 Months
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