- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07402967
Perceptions of Parents and Children on Posterior Restorations in Primary Molars
Perceptions of Parents and Children on Posterior Restorations in Primary Molars: An Institutional Study
The research on "Perceptions of Parents and Children on Posterior Restorations in Primary Molars at Universiti Teknologi MARA (UiTM)" gives valuable insights into what influences treatment choices in children's dental care. By understanding the worries and preferences of both parents and children, the study helps dentists better meet their needs, making the experience more comfortable. The findings enhance communication, promote informed decision-making, and ultimately improve patient satisfaction in children's dental care. For parents and children, participating in this research provides a clearer understanding of treatment options, ensures their preferences are considered and creates a more positive dental experience.
This research also helps improve paediatric dentistry overall, promoting family-centered care and guiding future dental practices and policies. The information gathered from this research will benefit individuals, researchers, institutions, and the community by advancing knowledge and informing future practices.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Selangor
-
Sungai Buloh, Selangor, Malaysia
- Universiti Teknologi MARA
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Children
- Children aged 5-12 years old.
- Paediatric patients who attended UiTM undergraduate clinic.
- Fit and healthy patient.
- Children who understand English or Malay.
Parents
- Parents/guardians who have provided consent to participate in the study.
- Parents who understand English or Malay.
- Only one parent for each child.
Exclusion Criteria:
Children
- Children below 5 years old and above 12 years old.
- Paediatric patients who attended other than UiTM undergraduate clinics.
- Children with disabilities.
- Children who do not understand English or Malay.
Parent
- Parents with children below 5 years old and above 12 years old.
- Parents/guardians who do not provide consent to participate in the study.
- Parents who do not understand English or Malay. -
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Children
Child aged from 5-12 years old
|
Questionnaire about their perception on dental restoration for paediatric posterior teeth
|
|
Parent
Parent who had child aged 5-12 years old
|
Questionnaire about their perception on dental restoration for paediatric posterior teeth
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental Preference for Posterior Restorations in Primary Molars
Time Frame: January 2025 until January 2026
|
Outcome Measure Description: Assessment of the parents' preferred choice of restoration using the study questionnaire (Domain 3.4: Perception). Parents are presented with 4 images representing different restoration options: Image A (Stainless steel crown), Image B (Amalgam restoration), Image C (Composite restoration), and Image D (Bioflex crown), and asked to select the single option they prefer. Unit of Measure: Percentage of participants |
January 2025 until January 2026
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental Income Level
Time Frame: january 2025 until January 2026
|
Outcome Measure Description: Assessment of the parents' socioeconomic status based on self-reported monthly income collected via the sociodemographic section of the study questionnaire. Unit of Measure: Malaysian Ringgit (MYR). Grouped into Monthly household income : Less than RM2499 RM2500 - RM4849 RM4850 - RM 10,959 More than RM11,000 |
january 2025 until January 2026
|
|
Age of Child
Time Frame: January 2025 until January 2026
|
Outcome Measure Description: Assessment of the paediatric patient's age collected via the sociodemographic section of the study questionnaire. Unit of Measure: Years (or months, as applicable) |
January 2025 until January 2026
|
|
Parental Education Level
Time Frame: January 2025 until January 2026
|
Outcome Measure Description: Assessment of the parents' highest level of education attained, collected via the sociodemographic section of the study questionnaire. Unit of Measure: Level of education No formal education Primary school Secondary school Tertiary school Postgraduate |
January 2025 until January 2026
|
|
Gender of Child
Time Frame: January 2025 until January 2026
|
Outcome Measure Description: Assessment of the paediatric patient's gender (e.g., male or female) collected via the sociodemographic section of the study questionnaire. Unit of Measure: Percentage of participants (e.g., % Male, % Female) |
January 2025 until January 2026
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Stomatognathic Diseases
- Tooth Diseases
- Tooth Demineralization
- Dental Caries
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Surveys and Questionnaires
Other Study ID Numbers
- ERC/01/2025 (ERP/4/19) (39)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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