- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06683144
Effects of Health Belief Model Interventions on Preventive Beliefs in Secondhand Smoke Exposure
February 12, 2025 updated by: Ercan Asi, Akdeniz University
Effects of Feedback, Education, and Social Media Interventions Based on the Health Belief Model on Preventive Beliefs in Adults Exposed to Secondhand Smoke At Home.
The aim of this study was to compare the effects of feedback, interactive education, and social media interventions based on the health belief model on protective beliefs in adults at risk of exposure to secondhand smoke at home.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Secondhand smoke (SHS) exposure, also known as environmental tobacco smoke, passive smoke or involuntary smoke, is caused by the burning of cigarettes and other tobacco products and the smoke exhaled by a smoker.
Although Turkey is one of the best countries in combating SHS exposure, one in four adults is exposed to SHS at home.
One of the most important reasons for this exposure is the lack of deterrent policies for the home environment, which is considered a private area.
It is entirely possible for non-smoking individuals to be protected from SHS exposure at home through their own efforts.
In this context, the knowledge, behaviors and perceptions of non-smoking adults about exposure are important in preventing or reducing SHS exposure at home.
Interventions based on the behavior change model can be effective in developing protective behaviors in adults at risk of SHS exposure at home.
Individual and group interventions using multiple educational materials and methods based on the Health Belief Model (HBM) (SHS exposure feedback, interactive group education and social media sharing) can develop protective behaviors in individuals at home.
Study Type
Interventional
Enrollment (Estimated)
93
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ercan Asi
- Phone Number: +905342087249
- Email: ercanasi@akdeniz.edu.tr
Study Locations
-
-
Konyaaltı
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Antalya, Konyaaltı, Turkey, 07070
- Akdeniz University Faculty of Nursing
-
Contact:
- Ercan Asi
- Phone Number: +905342087249
- Email: ercanasi@akdeniz.edu.tr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
İnclusion Criteria
- Non-smokers aged 18-64 who live with at least one smoker,
- Literate individuals,
- Individuals who own a smartphone,
- Individuals who voluntarily agree to participate in the study.
Exclusion Criteria:
- Individuals who do not speak Turkish,
- Pregnant individuals,
- Participants who have been living apart from SHS exposure sources in the week leading up to data collection.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exposure feedback group
|
|
|
Experimental: Interactive education group
|
Slide presentation, video presentation, Q&A, evaluation of learning and discussion of results
|
|
Experimental: Social media group
|
Sharing informational materials such as messages, brochures, and videos related to SHS exposure, including ways to protect yourself from SHS exposure and the adverse health effects of SHS exposure.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health belief model scale for prevention behaviors of secondhand smoke exposure (HBM-SHS)
Time Frame: Baseline and at first month later after intervention
|
The 35-item scale, scored on a five-point Likert scale from "Strongly Disagree (1)" to "Strongly Agree (5)," assesses six subdimensions: "perceived susceptibility," "perceived seriousness," "perceived benefits," "perceived barriers," "self-efficacy," and "behavioral cues."
Items on "perceived susceptibility" and "perceived barriers" are reverse coded.
Scores range from 35 to 175, with higher scores indicating stronger health beliefs about SHS exposure and greater beliefs in each subdimension.
|
Baseline and at first month later after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Secondhand Smoke Exposure Risk Assessment
Time Frame: Baseline and at first month later after intervention
|
Risk assessment is conducted through four questions addressing whether there is a smoker in the household, household tobacco use rules, tobacco use in enclosed areas, and the time since the last use.
Responses are scored categorically: absence of risk is scored as 0, while the presence and intensity of risk are scored as 1 or more.
A score of at least one indicates "risk."
SHS exposure risk is scored from 0 to 10, with any score of 1 or above indicating the presence of risk.
Total risk assessment scores are represented on a real risk scale of 0-10.
According to expert evaluations, the content validity index (CVI) of the questions assessing participants' SHS exposure risk level is 0.86.
|
Baseline and at first month later after intervention
|
|
Actual Risk Assessment
Time Frame: Baseline and at first month later after intervention
|
In adults at risk of SHS exposure, urinary cotinine analysis will be conducted using a cotinine urine test kit.
The test detects cotinine in the urine, indicating SHS exposure.
The strip is dipped into the urine sample for 10 seconds, and the result is read within 5 minutes.
In a negative result, both the control (C) and test (T) lines will appear, while in a positive result, only the control line (C) will appear.
If neither the C nor T lines are visible, or if only the T line appears, the test is invalid.
|
Baseline and at first month later after intervention
|
|
Perceived SHS Exposure Risk
Time Frame: Baseline and at first month later after intervention
|
In adults, SHS exposure risk will be assessed based on the perceived level of risk.
Participants' awareness of SHS exposure will be measured by their responses to the question, "How would you describe your risk of being exposed to SHS in your home?" with options such as "No risk at all," "Somewhat at risk," or "At very high risk."
Additionally, participants' perceived SHS exposure risk level will be evaluated based on their numerical responses to the question, "What would your risk of SHS exposure in your home be on a scale from 0 to 10?" Each number will represent the participant's perceived (exposure risk probability) risk.
|
Baseline and at first month later after intervention
|
|
ThirdHand Smoke Beliefs Scale (BATHS)
Time Frame: Baseline and at first month later after intervention
|
This scale was developed by Haardörfer and colleagues in 2017 to identify beliefs about third-hand smoke (THS).
The scale includes 5 items related to the health effects of THS and 4 items regarding its persistence in the environment.
The items are rated using a 5-point Likert scale, with the following coding: 5 = Strongly agree, 4 = Agree, 3 = Neutral, 2 = Disagree, 1 = Strongly disagree.
The total score of the scale is obtained by dividing the sum of the item scores by the number of items.
A score closer to 5 for each item indicates the individual believes in the health and environmental effects of THS, while a score closer to 1 indicates disbelief.
|
Baseline and at first month later after intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2025
Primary Completion (Estimated)
June 10, 2025
Study Completion (Estimated)
December 10, 2025
Study Registration Dates
First Submitted
November 8, 2024
First Submitted That Met QC Criteria
November 8, 2024
First Posted (Actual)
November 12, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 12, 2025
Last Verified
November 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AU-NF-EA-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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