Skip to main content
Clinical Trials/NCT04566159
NCT04566159
Completed
Not Applicable

Computer Delivered and Community Health Worker Supported Smoking Cessation Intervention for Hospitalized Persons With HIV

Johns Hopkins University1 site in 1 country22 target enrollmentJanuary 11, 2021
ConditionsTobacco Smoking

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tobacco Smoking
Sponsor
Johns Hopkins University
Enrollment
22
Locations
1
Primary Endpoint
Intervention Feasibility as assessed by the Feasibility of Intervention Measure
Status
Completed
Last Updated
5 months ago

Overview

Brief Summary

The prevalence of tobacco smoking is high among persons with HIV (PWH). The investigators are piloting a two session computer-delivered intervention (CBI) with linkage to a community health worker (CHW) among hospitalized PWH with tobacco use 1a) To determine feasibility and acceptability of delivering this intervention and 2a) To determine intervention effect on 1) readiness to quit smoking and confidence in ability to quit smoking 2) uptake of smoking cessation therapy

Registry
clinicaltrials.gov
Start Date
January 11, 2021
End Date
December 1, 2021
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \>=18,
  • A patient admitted to the Johns Hopkins Hospital
  • Smoked \>100 cigarettes in their lifetime
  • Current smoker
  • English speaking

Exclusion Criteria

  • Contraindication to nicotine replacement therapy including unstable angina and acute coronary syndrome

Outcomes

Primary Outcomes

Intervention Feasibility as assessed by the Feasibility of Intervention Measure

Time Frame: 3 months

4 item scale, maximum score of 20 with higher score indicating greater feasibility

Intervention Acceptability as assessed by the Acceptability of an Intervention Measure

Time Frame: 3 months

Noted as continuous score on 4 item scale, maximum value of 20 with higher score indicating greater acceptability

Secondary Outcomes

  • Continued use of nicotine replacement therapy 1 month post intervention(30 days post intervention)
  • Readiness to quit smoking as assessed by a Visual analog scale(immediately post intervention)
  • Uptake of nicotine replacement therapy(immediately post intervention)

Study Sites (1)

Loading locations...

Similar Trials