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Clinical Trials/PACTR202211868634078
PACTR202211868634078
Not yet recruiting
Phase 4

Integrating Tobacco use cessation into HIV Care and Treatment Clinics in Ministry of Health Facilities in Kisumu County, Kenya.

niversity of California San Francisco0 sites580 target enrollmentNovember 18, 2022
ConditionsHIV/AIDS

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
HIV/AIDS
Sponsor
niversity of California San Francisco
Enrollment
580
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 18, 2022
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of California San Francisco

Eligibility Criteria

Inclusion Criteria

  • Clinical Component (Randomized Control trial):
  • \-age \=18 years
  • \-HIV\-seropositive
  • \-on or initiating ART
  • \-not planning to move or travel within 12 weeks following entry in the study
  • \-Tobacco inclusion criteria: current tobacco users, i.e. used tobacco in the past 7 days; for smokers, smoked at least 100 cigarettes in lifetime, and at least 5 cigarettes per day, verified by expired Carbon Monoxide (CO)\= 5\-6 parts per million (ppm).
  • \-access to mobile phone for phone contact (and on intensive intervention also for text follow up visit)
  • Additional inclusion criteria for intensive intervention only:
  • \-able to read or be read for the SMS messages

Exclusion Criteria

  • Clinical Component:
  • \-age \< 18 years
  • \-HIV\-seronegative
  • \-unable to provide informed consent
  • \-unwilling to be contacted by clinic for follow up
  • \-Opioid users (who may be receiving Bupropion as part of their treatment)
  • Additional exclusion criteria for intensive intervention only:
  • \-Myocardial Infarction in the 2 weeks prior to enrolling in the study
  • \-Pregnant (as NRT and Bupropion might be contraindicated).
  • \-We will also exclude patients for whom Bupropion is contraindicated (e.g. history of seizures, recent use of MAO inhibitors, breastfeeding, and whose ART protocol present, as per prescription guidance, contraindications).

Outcomes

Primary Outcomes

Not specified

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