- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06670729
Alternatives to Manage Dental Fear
October 31, 2024 updated by: Abrar Nizar Al-Attar, Al-Mustansiriyah University
Psychotherapeutic Effect of Listening to Quran Recitation on Dental Anxiety: a Randomized Controlled Trial
This study compares the psychological effects on patients attend the dental clinic by listening to specific audios
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Participants of the experimental group listened to Quran recitation using auto-controlled headphones, whereas headphones of the control group participants were silent then the two groups answer questionnaire prepared for this purpose.
Study Type
Interventional
Enrollment (Actual)
30
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 Locations
-
-
-
Baghdad, Iraq, 964
- College of Dentistry
-
-
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
No
Description
Inclusion Criteria:
- any patient eligible for dental treatment
- willing to participate
Exclusion Criteria: participants
- less than 18 years of age,
- mentally retarded,
- had hearing impairment or deafness
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Quran listening group
participants listen to Quran recitation
|
listening to quran recitation via head phone
|
|
Other: silent headphones
participant's headphone is silent
|
headphones were silent, patient do not listen to any thing
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
fear
Time Frame: before, during and immediately after dental session
|
fear was assessed using a questionnaire that is based on Dental anxiety scale (DAS) and Modified Dental Anxiety scale (MDAS), statistically significant descending ranks of fear reflects effectiveness of the intervention, when statistical analysis was significant, clinical (practical) effect size was also obtained to determine the clinically effective modality of management
|
before, during and immediately after dental session
|
|
discomfort
Time Frame: during and immediately after dental session
|
presence or absence of discomfort was assessed using dental anxiety scale and modified dental anxiety scale, descending ranks of fear reflects effectiveness of the intervention
|
during and immediately after dental session
|
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 (Actual)
October 26, 2021
Primary Completion (Actual)
December 31, 2021
Study Completion (Actual)
December 31, 2021
Study Registration Dates
First Submitted
October 30, 2024
First Submitted That Met QC Criteria
October 31, 2024
First Posted (Estimated)
November 1, 2024
Study Record Updates
Last Update Posted (Estimated)
November 1, 2024
Last Update Submitted That Met QC Criteria
October 31, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC108
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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