Verbal and Visual Information Techniques on Anxiety in Third Molar Surgery

Sponsor

Konya Necmettin Erbakan Üniversitesi (Other)

Overall Status

Completed

CT.gov ID

NCT03752255

Collaborator

(none)

240

Enrollment

Location

Arms

Actual Duration (Days)

243.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The aim of this study was to evaluate preoperative anxiety levels using dental anxiety scale (DAS) and the Spielberger State-Trait Anxiety Inventory (STAI).

Condition or Disease	Intervention/Treatment	Phase
Impacted Third Molar Tooth	Other: Anxiety measurement method	N/A

Detailed Description

This study will based on a prospective, observational investigation of two different patient education techniques about the effect of third molar removal on patients' anxiety level. A total of 240 patients will be divided into two groups.

Information about operation procedures and a recovery will be given verbally in group 1 and information about operation procedures and recovery will be given in group 2. Anxiety levels were assessed by using DAS and (STAI).Paired t-test or Wilcoxon test will be used for intra-group comparison of anxiety levels.

Study Design

Study Type:

Interventional

Actual Enrollment :

240 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Single (Participant)

Primary Purpose:

Other

Official Title:

The Effects of Verbal and Visual Information Techniques on Anxiety in Impacted Third Molar Surgery

Actual Study Start Date :

Nov 21, 2018

Actual Primary Completion Date :

Dec 21, 2018

Actual Study Completion Date :

Dec 21, 2018

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Anxiety measurement method Before the operation, patients in the experimental group will fill the anxiety scales (DAS and STAI). Then patients will watch a video about impacted tooth. This video will include the complications that patients may face and what should be done after the procedure. After the watching the video, patients will fill the both DAS and STAI.	Other: Anxiety measurement method Two different techniques (video or verbal information) will be examined about impacted third molar surgery.
Placebo Comparator: Control Before the operation, patients in the experimental group will fill the anxiety scales (DAS and STAI). The verbal information in detail will be given to the patients by the surgeon.This verbal information will include the complications that patients may face and what should be done after the procedure.	Other: Anxiety measurement method Two different techniques (video or verbal information) will be examined about impacted third molar surgery.

Arm

Intervention/Treatment

Experimental: Anxiety measurement method

Before the operation, patients in the experimental group will fill the anxiety scales (DAS and STAI). Then patients will watch a video about impacted tooth. This video will include the complications that patients may face and what should be done after the procedure. After the watching the video, patients will fill the both DAS and STAI.

Other: Anxiety measurement method

Two different techniques (video or verbal information) will be examined about impacted third molar surgery.

Placebo Comparator: Control

Before the operation, patients in the experimental group will fill the anxiety scales (DAS and STAI). The verbal information in detail will be given to the patients by the surgeon.This verbal information will include the complications that patients may face and what should be done after the procedure.

Other: Anxiety measurement method

Two different techniques (video or verbal information) will be examined about impacted third molar surgery.

Outcome Measures

Primary Outcome Measures

The anxiety levels will be examined using DAS and STAI. [first day]
first day

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 60 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Impacted third molar (bone and mucosa retention, mesioangular position)
Patients with any chronic disease and allergy

Exclusion Criteria:

Pericoronitis
Patients with visual impairment
Patients with psychological disorders
Smoking
Pregnancy or lactation

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Necmettin Erbakan University	Konya	Karatay	Turkey	42050

Sponsors and Collaborators

Konya Necmettin Erbakan Üniversitesi

Investigators

Principal Investigator: Dilek Menziletoglu, Dr, Necmettin Erbakan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Dilek Menziletoglu, Principle Investigator, Konya Necmettin Erbakan Üniversitesi

ClinicalTrials.gov Identifier:

NCT03752255

Other Study ID Numbers:

NEU2

First Posted:

Nov 23, 2018

Last Update Posted:

Dec 26, 2018

Last Verified:

Nov 1, 2018

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by Dilek Menziletoglu, Principle Investigator, Konya Necmettin Erbakan Üniversitesi

Video

Anxiety

Additional relevant MeSH terms:

Tooth, Impacted

Study Results

No Results Posted as of Dec 26, 2018