Feasibility and Acceptability of Oxygen Saturation Monitoring Using Masimo SafetyNet Alert (MSNA) in a Supportive Housing Program

Masimo

Status

Terminated

Conditions

Opioid Use

Treatments

Device: Masimo SafetyNet Alert (MSNA)

Study type

Interventional

Funder types

Industry

Identifiers

NCT06217380

SAFE0004

Details and patient eligibility

About

This Clinical Trial will evaluate the Feasibility and Acceptability of Oxygen Saturation Monitoring using Masimo SafetyNet Alert (MSNA) in a Supportive Housing Program

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Client Participants:

Participants who are18 years of age or greater
Participants housed within a supportive housing program who intend to inject opioids
Participants who have given verbal informed consent to participate in the study

Inclusion Criteria for Staff Participants:

Participant is research staff and/or Rita Thompson Residence staff
Participant is willing to give implied consent by reading and completing the staff survey

Exclusion Criteria for Client Participants:

Participants deemed not suitable for the study at the discretion of the principal investigator, research staff or housing program nurses/staff
Participants with skin abnormalities at the planned application sites that may interfere with sensor application, per directions-for-use (DFU) or trans-illumination of the site, such as psoriasis, eczema, angioma, burns, scar tissue, substantial skin breakdown, nail polish, acrylic nails, infections, or other abnormalities that may interfere with MSNA functioning
Participants with known allergic reactions to foam/rubber products and/or adhesive tape

Exclusion Criteria for Staff Participants:

-None