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Clinical Trials/NCT03927976
NCT03927976
Completed
Not Applicable

Testing the Feasibility of a Culturally-Specific Video Text Cessation Intervention With African American Quitline Callers

Case Comprehensive Cancer Center1 site in 1 country35 target enrollmentApril 10, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tobacco Use Cessation
Sponsor
Case Comprehensive Cancer Center
Enrollment
35
Locations
1
Primary Endpoint
Feasibility as measured by interest in using Path2Quit video text program
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Assess the feasibility and acceptability of delivering an mHealth tobacco intervention among state quitline enrollees.

Detailed Description

The main objective of this study is to assess the feasibility of delivering an mHealth tobacco intervention among state quitline enrollees. This will be measured through the assessment of interest and willingness to use the video text program, and the ability to receive video text messages (i.e., has technology capable of receiving and viewing video texts. At the end of the intervention, the team will assess satisfaction and perceived helpfulness of the video-text messaging program as an indication of acceptability.

Registry
clinicaltrials.gov
Start Date
April 10, 2019
End Date
February 10, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Self-identify as African American
  • Enrolled in state quitlines within the past 3 months
  • Have access to SMS texting

Exclusion Criteria

  • Does not meet inclusion criteria

Outcomes

Primary Outcomes

Feasibility as measured by interest in using Path2Quit video text program

Time Frame: Through study completion, an average of 6-weeks.

The program will be evaluated as feasible if 50% of those screened are eligible and interested in the video text program AND if 90% of those who are eligible and interested in the video text program will be able to engage in the program (some may need technical assistance).

Secondary Outcomes

  • Acceptability of intervention in terms of its Satisfaction and perceived helpfulness: 6-Week Follow-Up Questionnaire(6 weeks from end of intervention)

Study Sites (1)

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