"The Effect of Lavender Aromatherapy on Dental Anxiety"

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-45
SponsorDow University of Health Sciences

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Lavender Aromatherapy

    Other intervention

    Lavender Aromatherapy will administrated to Experimental group

  • Placebo Control

    Other intervention

    The control group will receive placebo intervention via nebulizer filled with normal saline for 15 minutes to remain calm and anxiety free.

Treatment groups

68 Participants
are divided into 2 treatment groups
Group A: Experimental: Aromatherapy will be administered.Experimental treatment 1 intervention
Group B: Group 2: (Control): Placebo interventionPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

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

Time frame
one hour

Secondary outcomes

1

Physiological Parameters

Both Systolic and Diastolic Blood pressure measured in mm of Hg. .

Time frame
One hour
2

Physiological Parameter

Pulse rate measured as beats per minutes (BPM)

Time frame
one hour
3

Physiological Parameter

Oxygen saturation measured in %

Time frame
one hour

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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