Skip to main content
Clinical Trials/NCT07734727
NCT07734727Not yet recruitingNot Applicable

Adaptation and Testing of a Novel Text-based Tobacco Cessation and Education Intervention in Kenyan Emergency Department Patients

Yale University1 site in 1 country285 target enrollmentStarted: August 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
285
Locations
1
Primary Endpoint
Exhaled Carbon Monoxide testing to assess efficacy

Study Overview

Brief Summary

In this study, investigators will adapt and implement Text2Quit in a Kenyan ED population will increase knowledge and cessation. Investigators will use a mixed-methods, hybrid implementation-effectiveness approach to assess these outcomes. Results will inform a randomized, controlled trial in a nationally representative sample of EDs in future. This study will be the first to target tobacco use in this population, the first to use mobile cessation, and will contribute to advancing implementation science on tobacco cessation globally. It will also provide a novel approach to implementation for mHealth interventions, with findings that can be generalized to other Non-Communicable Diseases and risk factors, such as alcohol use, hypertension and diabetes.

Detailed Description

Aim 1. To assess tobacco use and willingness to engage with mHealth for tobacco cessation targeting Kenyan ED patients.

Aim 2. To adapt the Text2Quit mHealth tool for use in the Kenya context using a participatory approach.

Aim 3. To pilot test Text2Quit-Kenya and assess its acceptability, feasibility, and efficacy.

The focus of this registration is Aim 3.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Current tobacco users (self-identified smokers).
  • •Presenting to the Emergency Department (ED) at Kenyatta National Hospital (KNH).
  • •Own a mobile phone capable of receiving text messages.
  • •Willing to quit tobacco use.
  • •Able and willing to provide informed consent.

Exclusion Criteria

  • •Individuals unwilling or unable to provide consent.
  • •Non-tobacco users.
  • •Those without access to a mobile phone.
  • •Patients who are critically ill or otherwise unable to participate (practically excluded at triage).

Arms & Interventions

Control

No Intervention

Standard of care

Text2Quit Kenya

Active Comparator

Participants will receive the Text2Quit intervention

Intervention: Text2Quit-Kenya (Other)

Outcomes

Primary Outcomes

Exhaled Carbon Monoxide testing to assess efficacy

Time Frame: Baseline, Month 1 and Month 6

Efficacy will be assessed by repeat exhaled Carbon Monoxide testing. Will be assessed using both a binary assessment with a cutoff of 10% and a continuous assessment of percent point prevalence

Text2Quit Survey to assess efficacy

Time Frame: Baseline and 1 Month post intervention

Efficacy will be assessed by self-report binary quantitative outcome of tobacco use in past 7 days

Secondary Outcomes

  • Percent enrollment(Baseline)
  • Tobacco Use Frequency(Baseline and Month 1)
  • Adoption assessed using Adoption RE-AIM Framework(up to Month 6)
  • Facililtators -Implementation(up to Month 6)
  • Barriers-Implementation(up to Month 6)
  • Frequency of message delivery(up to Month 6)
  • Frequency of message read(Baseline, Month 1 and Month 6)
  • Frequency of response(up to Month 6)
  • Maintenance assessed using RE-AIM Framework(Month 6)
  • Cost(Month 6)
  • Tobacco Policies Knowledge(Baseline and Month 1)
  • Tobacco Harms Knowledge(Baseline and Month 1)
  • Mean Tobacco Cessation Attempts(Baseline and Month 1)
  • Absolute Number Tobacco Cessation Attempts(Baseline and Month 1)

Investigators

Sponsor
Yale University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials