- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07699341
Training on the Heimlich Maneuver for Mothers of Children With Disabilities
July 9, 2026 updated by: Emel AVÇİN, University of Yalova
For a Safe Breath: Training on the Heimlich Maneuver for Mothers of Children With Disabilities in Cases of Foreign Body Obstruction
Foreign body obstruction is one of the most common causes of medical emergencies, particularly in childhood, and can lead to fatal outcomes if not treated promptly and correctly.
Therefore, this study aims to examine the effect of hands-on Heimlich maneuver training for mothers of children with disabilities on the mothers' knowledge, skills, self-efficacy, and anxiety levels.
Conducted as a randomized controlled trial, the study is planned to include 70 mothers (experimental group: 35, control group: 35) of children aged 1-8 years attending a private rehabilitation center in the Besni district of Adıyaman.
Data collection tools will consist of a demographic information form, a Heimlich maneuver knowledge and skill test, and self-efficacy and anxiety scales.
A pilot study will be conducted to evaluate the validity and reliability of the data collection tools, test their comprehensibility for the mothers, and identify potential problems that may arise during implementation.
Prior to the start of the training, the knowledge levels of all mothers will be assessed via a questionnaire.
The Heimlich maneuver training provided to mothers in the experimental group will be delivered hands-on using a pediatric Heimlich mannequin.
One month after the training, a post-test will be administered to the mothers.
Mothers in the control group will be informed about the study during the initial interview and will take a pre-test.
One month after the training, the mothers will take the post-test.
Mothers in the control group will be informed about the study during the initial interview and will take the pre-test.
The post-test will be administered one month later, after which the mothers in this group will also receive maneuver training.
The mothers' pre-test and post-test scores will be compared both within and between groups.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
70
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: EMEL AVÇİN, Assist Prof
- Phone Number: 05534524243
- Email: emel.avcin@hotmail.com
Study Locations
-
-
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Adıyaman, Turkey (Türkiye), 02400
- Recruiting
- Emel Avçin
-
Contact:
- Ali Tekin
- Phone Number: 05534524243
- Email: emel.avcin@hotmail.com
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-
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
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Be a mother of a child with a disability, aged 1-8, who is enrolled in a rehabilitation center.
- Be 18 years of age or older.
- Be able to read and understand the research protocol, provide written informed consent, and agree to participate.
- Be physically able to participate in the training (standing/model-based exercises).
Exclusion Criteria:
- Must have previously received professional Heimlich maneuver/first aid training (those who have taken a course within the last 2 years).
- Those who are unable to participate in hands-on training due to physical limitations (e.g., severe heart disease, mobility issues).
- Individuals determined to be unsuitable for training or assessments due to psychiatric or neurological conditions.
- Children with severe respiratory system disorders (e.g., tracheostomy, severe bronchopulmonary dysplasia),
- Children who have undergone heart surgery or have a serious cardiac anomaly,
- Children with severe orthopedic or neurological disabilities for whom performing the Heimlich maneuver may be risky,
- Children with congenital anomalies of the trachea or upper respiratory tract (e.g., tracheoesophageal fistula),
- Children requiring mechanical ventilator support or continuous oxygen therapy.
- Withdrawing from participation during the study or failing to attend any of the training/testing sessions.
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: intervention group
Mothers in the experimental group will receive training on how to perform the Heimlich maneuver for foreign-body obstruction in children with disabilities.
The training will include theoretical instruction and hands-on demonstrations using a mannequin.
Each mother will first receive theoretical and practical instruction, then be asked to perform the maneuver, and her performance will be evaluated through a skills test.
She will continue practicing until she performs the maneuver correctly.
Training will be provided one-on-one to each mother in a room assigned by the institution, lasting an average of 30-45 minutes.
A visually supported informational guide will be shared via cell phone so that mothers can refer to it as needed.
The practical steps in this training are based on the first aid guidelines of the American Academy of Pediatrics and the Ministry of Health of the Republic of Turkey.
The Heimlich Maneuver for children covers children aged 1-8 years (APA, 2017).
|
The Heimlich Maneuver training materials were prepared based on the first aid guidelines of the American Academy of Pediatrics and the Ministry of Health of the Republic of Turkey.
A guide supported by visuals was also prepared to serve as a reminder.
The training was demonstrated hands-on using a mannequin, and participants then practiced the technique under the supervision of a parent.
|
|
No Intervention: Control group
Mothers in the control group do not receive the training provided to the experimental group.
However, these mothers are asked not to receive any external Heimlich Maneuver training during the study period.
Once all data collection and analysis processes are complete, mothers in the control group will also receive the same high-quality Heimlich Maneuver training free of charge.
A visually supported informational guide will be shared via cell phone so that mothers can refer to it when needed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heimlich Knowledge Test
Time Frame: Baseline, Week 4, and Week 8
|
Parental first aid knowledge was assessed using a researcher-developed 12-item multiple-choice knowledge test.
The test includes questions on recognition of foreign body obstruction, correct first aid steps, calling for emergency assistance, and age-group-specific application knowledge.
Each correct answer was scored as 1 point and incorrect answers as 0 points.
Total scores range from 0 to 12, with higher scores indicating better first aid knowledge.
|
Baseline, Week 4, and Week 8
|
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Parental Self-Efficacy Scale
Time Frame: Baseline, Week 4, and Week 8
|
Parental self-efficacy was assessed using the Parental Self-Efficacy Scale.
The scale consists of 17 items rated on a 7-point Likert scale.
Total scores range from 17 to 119, with higher scores indicating higher parental self-efficacy.
|
Baseline, Week 4, and Week 8
|
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Beck Anxiety Inventory Score
Time Frame: Baseline, Week 4, and Week 8
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Anxiety symptoms were assessed using the Beck Anxiety Inventory.
The scale consists of 21 items rated on a 4-point Likert scale.
Each item is scored from 0 to 3, resulting in a total score ranging from 0 to 63.
Higher total scores indicate greater severity of anxiety symptoms.
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Baseline, Week 4, and Week 8
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: EMEL AVÇİN, Assist Prof, Adiyaman University
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 (Actual)
June 1, 2016
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
November 30, 2026
Study Registration Dates
First Submitted
July 4, 2026
First Submitted That Met QC Criteria
July 9, 2026
First Posted (Actual)
July 13, 2026
Study Record Updates
Last Update Posted (Actual)
July 13, 2026
Last Update Submitted That Met QC Criteria
July 9, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Heimlich Ma.
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data (IPD) will not be shared.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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