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CompletedNCT07917286Updated Nov 4, 2026

Comparison of the Effectiveness of Oral Hygiene Motivation Methods Among Dentistry and Psychology Students

An interventional study of Verbal Motivation and Model Demonstration in Oral Hygiene Motivation, Oral Hygiene and Dental Plaque, sponsored by Cyprus Health and Social Sciences University. Completed at 1 site in Cyprus. Open to participants aged 18 Years to 28 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-04.

Sponsored by Cyprus Health and Social Sciences University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Dec 2025, registered Oct 2026).
Updated Nov 4, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 28 Years
Sex
All
01

Study summary

This study aimed to compare the short-term effects of three oral hygiene motivation methods on dental plaque accumulation and gingival inflammation among Dentistry and Psychology students. It also aimed to evaluate whether the effects of these methods differed according to academic department.

This randomized clinical trial included 120 students aged 18-28 years who were enrolled in the Dentistry and Psychology departments at Cyprus Health and Social Sciences University. Participants were randomly assigned within each department to one of three oral hygiene motivation methods: verbal instruction, dental model demonstration, or plaque-disclosing agent-supported motivation.

All participants received the same standardized oral hygiene content, information leaflet, toothbrush, and toothpaste, while the motivational approach differed between groups. Professional scaling and polishing were also performed for all participants. The Silness-Löe Plaque Index (PI) and Löe-Silness Gingival Index (GI) were recorded at baseline and three weeks after the intervention.

The study evaluated changes in plaque and gingival indices to compare the effectiveness of the three motivation methods and assess whether their effects differed between Dentistry and Psychology students.

Read the detailed description

This single-center randomized clinical trial was conducted among Dentistry and Psychology students at Cyprus Health and Social Sciences University between December 2025 and February 2026. The primary aim was to compare the short-term effects of three oral hygiene motivation methods on plaque accumulation and gingival inflammation. The secondary aim was to evaluate whether the effects of these methods differed between Dentistry and Psychology students.

A total of 120 students aged 18-28 years participated in the study, including 60 Dentistry students and 60 Psychology students. Within each academic department, participants were randomly allocated to one of three motivation methods using computer-generated random allocation sequences. Six study groups were formed, each consisting of 20 participants.

At baseline (T0), plaque accumulation and gingival inflammation were assessed using the Silness-Löe Plaque Index (PI) and Löe-Silness Gingival Index (GI), respectively. Following these assessments, the assigned motivation intervention was delivered in a single session. All participants received the same standardized core oral hygiene information covering dental plaque, toothbrushing, and interdental cleaning. However, the groups differed in how this information was delivered and in the motivational approach used. In the verbal motivation group, the information was delivered verbally. In the dental model demonstration group, the same information was demonstrated on a dental model. In the plaque-disclosing agent-supported group, dental plaque was visualized intraorally using a plaque-disclosing tablet, and individualized visual feedback was provided using a mirror.

After completion of the group-specific motivation interventions, all participants underwent professional scaling and polishing on the same day. All participants also received the same standardized oral hygiene information leaflet, toothbrush, and toothpaste. No additional motivational intervention or reminder was provided during the three-week follow-up period.

Clinical measurements at baseline (T0) and three weeks after the intervention (T1) were performed by a separate examiner who was unaware of the participants' group assignments. Changes in plaque and gingival indices were evaluated to compare the effects of the three motivation methods. Additionally, the study examined whether these effects differed between Dentistry and Psychology students.

02

Conditions studied

  • Oral Hygiene Motivation
  • Oral Hygiene
  • Dental Plaque

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Keywords

  • Oral hygiene motivation methods
  • Plaque index
  • Gingival index
  • Plaque-disclosing agent
  • University students
03

In context

Dental Plaque

352 studies on the registry are indexed under Dental Plaque; 60 are open to participants now.

This study's enrollment of 120 is above the median of 56 across 316 interventional studies indexed under Dental Plaque.

Browse Dental Plaque studies →

Lead sponsor

Cyprus Health and Social Sciences University is the lead sponsor of 4 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 28 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Students aged 18-28 years.
  • Enrollment in the Dentistry or Psychology department at Cyprus Health and Social Sciences University.
  • Voluntary agreement to participate in the study.
  • Provision of written .

Exclusion criteria

Exclusion Criteria:

  • Presence of systemic disease.
  • Ongoing orthodontic treatment.
  • Periodontal or oral conditions that could affect plaque and gingival index measurements.
  • Clinical findings consistent with periodontitis.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    Dentistry - Verbal Motivation

    This arm included 20 Dentistry students. At baseline (T0), plaque and gingival indices were measured before the intervention. Participants then received standardized oral hygiene education delivered verbally, together with a standardized oral hygiene information leaflet. Following the motivation intervention, professional scaling and polishing were performed, and participants received the same toothbrush and toothpaste as the other study groups. Plaque and gingival indices were reassessed three weeks after the intervention (T1).

    Behavioral: Verbal Motivation

  • Experimental
    Dentistry - Model Demonstration

    This arm included 20 Dentistry students. At baseline (T0), plaque and gingival indices were measured before the intervention. The researcher then demonstrated the standardized oral hygiene content, which was identical across all study groups, on a dental model. Participants also received the same standardized oral hygiene information leaflet provided to all groups. Following the motivation intervention, professional scaling and polishing were performed, and participants received the same toothbrush and toothpaste as the other study groups. Plaque and gingival indices were reassessed three weeks after the intervention (T1).

    Behavioral: Model Demonstration

  • Experimental
    Dentistry - Plaque Disclosing

    This arm included 20 Dentistry students. At baseline (T0), plaque and gingival indices were measured before the intervention. Participants then received standardized oral hygiene education supported by intraoral application of TePe PlaqSearch™ plaque-disclosing tablets. The disclosed plaque areas were shown to participants using a mirror, inadequately cleaned areas were pointed out, and individualized visual feedback was provided. Participants also received the same standardized oral hygiene information leaflet as all other groups. Following the intervention, professional scaling and polishing were performed, and participants received the same toothbrush and toothpaste as the other groups. Plaque and gingival indices were reassessed three weeks after the intervention (T1).

    Behavioral: Plaque Disclosing

  • Experimental
    Psychology - Verbal Motivation

    This arm included 20 Psychology students. At baseline (T0), plaque and gingival indices were measured before the intervention. Participants then received standardized oral hygiene education delivered verbally, together with a standardized oral hygiene information leaflet. Following the motivation intervention, professional scaling and polishing were performed, and participants received the same toothbrush and toothpaste as the other study groups. Plaque and gingival indices were reassessed three weeks after the intervention (T1).

    Behavioral: Verbal Motivation

  • Experimental
    Psychology - Model Demonstration

    This arm included 20 Psychology students. At baseline (T0), plaque and gingival indices were measured before the intervention. The researcher then demonstrated the standardized oral hygiene content, which was identical across all study groups, on a dental model. Participants also received the same standardized oral hygiene information leaflet provided to all groups. Following the motivation intervention, professional scaling and polishing were performed, and participants received the same toothbrush and toothpaste as the other study groups. Plaque and gingival indices were reassessed three weeks after the intervention (T1).

    Behavioral: Model Demonstration

  • Experimental
    Psychology - Plaque Disclosing

    This arm included 20 Psychology students. At baseline (T0), plaque and gingival indices were measured before the intervention. Participants then received standardized oral hygiene education supported by intraoral application of TePe PlaqSearch™ plaque-disclosing tablets. The disclosed plaque areas were shown to participants using a mirror, inadequately cleaned areas were pointed out, and individualized visual feedback was provided. Participants also received the same standardized oral hygiene information leaflet as all other groups. Following the intervention, professional scaling and polishing were performed, and participants received the same toothbrush and toothpaste as the other groups. Plaque and gingival indices were reassessed three weeks after the intervention (T1).

    Behavioral: Plaque Disclosing

Interventions

  • BehavioralVerbal Motivation

    Participants received a single session of standardized oral hygiene education delivered verbally after baseline plaque and gingival index measurements. The education covered oral hygiene, dental plaque, toothbrushing, and interdental cleaning, including recommendations to brush twice daily for two minutes and use dental floss daily. The same standardized oral hygiene information leaflet was provided to all study groups. Following the motivation session, participants underwent professional scaling and polishing and received the same toothbrush and toothpaste as the other groups. No additional motivational intervention or reminder was provided during the three-week follow-up period.

  • BehavioralModel Demonstration

    Participants received a single session of standardized oral hygiene education demonstrated by the researcher on a dental model after baseline plaque and gingival index measurements. The education covered oral hygiene, dental plaque, toothbrushing, and interdental cleaning, including recommendations to brush twice daily for two minutes and use dental floss daily. The same standardized oral hygiene information leaflet was provided to all study groups. Following the motivation session, participants underwent professional scaling and polishing and received the same toothbrush and toothpaste as the other groups. No additional motivational intervention or reminder was provided during the three-week follow-up period.

  • BehavioralPlaque Disclosing

    Participants received a single session of standardized oral hygiene education supported by intraoral application of TePe PlaqSearch™ plaque-disclosing tablets after baseline plaque and gingival index measurements. Disclosed plaque areas were shown using a mirror, inadequately cleaned areas were pointed out, and individualized visual feedback was provided. The education included recommendations to brush twice daily for two minutes and use dental floss daily. The same standardized oral hygiene information leaflet was provided to all study groups. Following the motivation session, participants underwent professional scaling and polishing and received the same toothbrush and toothpaste as the other groups. No additional motivational intervention or reminder was provided during the three-week follow-up period.

06

What researchers measure

Primary outcomes

  1. Change in Plaque Index (Silness-Löe) from Baseline to Three Weeks

    Dental plaque accumulation was assessed using the Silness-Löe Plaque Index (1964). The buccal/facial, lingual, mesial, and distal surfaces of all evaluable teeth, excluding third molars, were scored on a scale from 0 (no plaque) to 3 (abundant plaque accumulation). The mean score across evaluated sites was calculated for each participant. Change was calculated as the three-week score minus the baseline score (T1-T0). Negative values indicate a reduction in plaque accumulation.

    Time frame: Baseline (T0) and 3 weeks after intervention (T1)

  2. Change in Gingival Index (Löe-Silness) from Baseline to Three Weeks

    Gingival inflammation was assessed using the Löe-Silness Gingival Index (1963). The distofacial papilla, facial gingival margin, mesiofacial papilla, and lingual gingival margin of all evaluable teeth, excluding third molars, were scored on a scale from 0 (normal gingiva) to 3 (severe inflammation). The mean score across evaluated sites was calculated for each participant. Change was calculated as the three-week score minus the baseline score (T1-T0). Negative values indicate a reduction in gingival inflammation.

    Time frame: Baseline (T0) and 3 weeks after intervention (T1)

07

Study locations

1 site
  • Cyprus Health And Social Sciences University
    Mórfou, 99750, Cyprus
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Dec 2025 to primary completion in Feb 2026, 2 months.

Of 133 non-industry interventional studies with no phase under Dental Plaque, half reached primary completion within 7 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 16. This study's 2 months is below that.

Counting every sponsor, half of 178 studies reached it within 6 months; a quarter within 2 and three quarters within 14.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 29, 2026
First posted
Nov 4, 2026
StartActual
Dec 2, 2025
Primary completionActual
Feb 27, 2026
CompletionActual
Feb 27, 2026
Last update
Nov 4, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 4, 2026
Show all 1 update
  1. Nov 4, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07917286
Lead sponsor
Cyprus Health and Social Sciences University
Responsible party
Gizem Demirkaya (PhD Student, Cyprus Health and Social Sciences University) — Principal investigator
First posted
Nov 4, 2026
Start date
Dec 2, 2025
Primary completion
Feb 27, 2026
Completion
Feb 27, 2026
Last update
Nov 4, 2026

Study contacts

Gizem Demirkaya, DDS
principal investigator · Cyprus Health and Social Sciences University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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