Effects Of Training On Brushing Behavior

Sponsor
Okan University (Other)
Overall Status
Completed
CT.gov ID
NCT04018534
Collaborator
Fethiye Cakmak Ozlu (Other), Erol Aktunc (Other), Ersan Ilsay Karadeniz (Other)
90
3
54.7

Study Details

Study Description

Brief Summary

This study is a single-blind randomized controlled trial on fixed orthodontic appliance candidates (n = 90) assigned into a control group (n = 30) and two different study groups (n = 30 in each). Patients who requiring non-extraction fixed orthodontic treatment, crowding under 5mm in the incisors and heaving at least 20 permanent teeth with healthy periodontal tissue and devoid of caries were included in the study. The control group received a standard printed educational material assisted with verbal information. The study groups either received video assisted or hands-on training about fixed orthodontic appliance and oral hygiene. The time requirements for all three educational interventions were recorded at the initial visit. The adequacy of oral hygiene is documented through plaque and gingival indices at the initial visit and 8th week of the treatment.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Standard Verbal/Written Education
  • Behavioral: Video Assisted Education
  • Behavioral: Hands-on Training
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
90 consecutive fixed orthodontic appliance treatment candidates in compliance with the above mentioned criteria were randomly assigned to 3 groups (n = 30 in each); Control group: The patients in control group received a standard printed educational material assisted with verbal information in accordance with BOS educational goals. Study group 1: The patients in one of the study groups received a video assisted education . Study group 2: The patients in other study group received a hands-on training.90 consecutive fixed orthodontic appliance treatment candidates in compliance with the above mentioned criteria were randomly assigned to 3 groups (n = 30 in each); Control group: The patients in control group received a standard printed educational material assisted with verbal information in accordance with BOS educational goals. Study group 1: The patients in one of the study groups received a video assisted education . Study group 2: The patients in other study group received a hands-on training.
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effectiveness of Three Different Types Educational Methods on Implementation of Proper Oral Hygiene Behaviour Prior to Orthodontic Treatment
Actual Study Start Date :
May 5, 2014
Actual Primary Completion Date :
Jun 6, 2016
Actual Study Completion Date :
Nov 24, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Control group

The patients in control group received a standard printed educational material assisted with verbal information in accordance with British Orthodontics Society(BOS) educational goals.

Behavioral: Standard Verbal/Written Education
This patients as control group received a standard printed educational material assisted with verbal information in accordance with British Orthodontics Society (BOS) educational goals.

Experimental: Video assisted education group

The patients in one of the study groups received a video assisted education

Behavioral: Video Assisted Education
The video training consisted of two separate sessions, each one lasting 5 minutes, one about the treatment materials and the other about the oral hygiene successively and in compliance with the British Orthodontics Society (BOS) educational obligations. All of the candidates were allowed to rewind and watch the video presentation until they reach all of the educational goals. The accomplishment of the educational goals was documented through a written examination form filled in by the candidates themselves. All of the candidates have rated fullscore in the written examinations on both topics.

Experimental: Hands-on training group

The patients in other study group received a hands-on training.

Behavioral: Hands-on Training
The hands-on training consisting of two separate sessions was performed by one of the authors (E.A). The first is about the treatment materials and the second one is about the oral hygiene successively. They are in accordance with the British Orthodontics Society (BOS) educational obligations. All of the patients were allowed to ask questions freely until they reach all of the educational goals. The accomplishments of the educational goals were documented through a written examination form filled in by the candidates themselves. All of the candidates have rated fullscore in the written examinations on both topics. The time requirements for all three different educational interventions were recorded separately.

Outcome Measures

Primary Outcome Measures

  1. Plaque index(PI) for oral health assessment. [PI was measured at the 8 weeks later in each patient.]

    The brushing habits of the patients were checked at each appointment and were recorded with PI. This measurement of the state of oral hygiene by Silness-Löe plaque index is based on recording both soft debris and mineralized deposits on the following teeth.

  2. Gingival index(GI) for oral health assessment. [GI was measured at the 8 weeks later in each patient.]

    This index was used to assess the severity and prevalence of gingivitis.Probe was used as a sensor for GI scoring and the mesial, distal, buccal and lingual surfaces of the teeth were evaluated in patients undergoing fixed orthodontic treatment.

Secondary Outcome Measures

  1. Time duration spent for educational interventions [Average 30 minutes]

    The time requirements for all three different educational interventions were recorded separately.These time durations consisted of the education time needed for both fixed appliance components and oral hygiene educations all together.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 22 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Required non-extraction fixed orthodontic treatment, agree to use conventional stainless steel brackets (Gemini series; 3M Unitek, Monrovia, California, USA), at least 20 natural permanent teeth, crowding under 5 mm in the incisors and willing to participate in our research
Exclusion Criteria:
  • Dental caries, periodontal disease, systemic or chronic diseases such as diabetes, physical or mental disorders, smoking, previous orthodontic treatment, extensive dental restorations, antibiotic use during the previous 3 months, dental fluorosis and use of powered tooth brushes.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Okan University
  • Fethiye Cakmak Ozlu
  • Erol Aktunc
  • Ersan Ilsay Karadeniz

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hakan Yilmaz, Assistant Professor, Okan University
ClinicalTrials.gov Identifier:
NCT04018534
Other Study ID Numbers:
  • 11022014
First Posted:
Jul 12, 2019
Last Update Posted:
Jul 12, 2019
Last Verified:
Jul 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 12, 2019