About this trial
ABSTRACT
Background:
Dental anxiety is addressed as a common issue in adults, often delaying necessary dental treatments and impacting overall oral health. Conventional anxiety management methods may not be preferred due to certain limitations, therefore prompting interest in complementary therapies. The most promising therapy is aromatherapy. Aromatherapy uses essential oils for relaxation to reduce stress. This approach is non-invasive and accessible, making it a promising option for reducing dental anxiety. This study will examine the effect of aromatherapy in adults undergoing dental treatment, highlighting holistic strategies in dental care.
Aim of the study:
This study aimed to determine the effect of aromatherapy on dental anxiety among dental patients.
Methodology:
The study will be a randomized control trial, with 68 participants divided into two groups, Experimental (aromatherapy) and Control, randomizing through Sequentially Numbered, Opaque, and Sealed Envelopes (SNOSE). This trial will be conducted at dental OPD, Dr. Ishrat ul Ebad Khan Institute of Oral Health Sciences. The patients of both gender aged 20-45 years, requiring any dental procedure and providing an informed consent form will be part of the study. Patients with colds, asthma, or other respiratory diseases, acoustic problems, allergic to lavender oils used in the study and mental and physical disabilities will be excluded. It will be a single-blinded study where the examiner is unaware of group allocation. Questionnaires will be used to evaluate patient anxiety levels before the intervention and after dental procedure. Intervention (Aromatherapy) will be administered via nebulizer for 15 minutes. The control group will receive placebo intervention via nebulizer filled with normal saline for 15 minutes. Physiological data will be collected to measure stress response, including systolic and diastolic blood pressure, pulse rate, and oxygen saturation, using a digital sphygmomanometer and pulse oximeter at the start of the intervention (baseline) and at the end of the dental procedure.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients who will give consent to the study.
Patients aged 20-45 years undergoing dental treatment for the first time.
Both gender.
Patient seeking any one of the following dental procedures: root canal treatment, scaling and polishing or tooth extraction.
Disqualifiers
Patients with colds, asthma, and any other respiratory diseases.
Patients with acoustic problems.
Patients who are allergic Lavender oils that have been used in this study.
Patients with mental and physical disabilities.
Trial design
Parallel
Treatments tested in this trial
Lavender Aromatherapy
Other interventionLavender Aromatherapy will administrated to Experimental group
Placebo Control
Other interventionThe control group will receive placebo intervention via nebulizer filled with normal saline for 15 minutes to remain calm and anxiety free.
Treatment groups
Trial outcomes
Primary outcomes
Dental anxiety
Dental Anxiety status measured by Modified Dental anxiety scale. The minimum and maximum values recorded by Modified dental anxiety scale will be \< 10 and \>19 respectively and the higher scores means high dental anxiety which is worse outcome
Secondary outcomes
Physiological Parameters
Both Systolic and Diastolic Blood pressure measured in mm of Hg. .
Physiological Parameter
Pulse rate measured as beats per minutes (BPM)
Physiological Parameter
Oxygen saturation measured in %
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: