The Impact of Medical Play in the Dental Clinic Setting on the Cooperation of Neurotypical Patients

Sponsor
University of Colorado, Denver (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05571423
Collaborator
(none)
100
1
2
36
2.8

Study Details

Study Description

Brief Summary

The purpose of this pilot study is to investigate the efficacy of medical play in the dental setting to improve the behaviors and cooperation of neurotypical patients during dental visits.

The specific aims of the study are as follows:
  1. To evaluate differences in behaviors and cooperation levels of subjects utilizing medical play before a routine dental exam visit in comparison to those undergoing a routine dental exam visit without use of medical play.

  2. To evaluate whether subjects who have a dental exam visit, with or without use of medical play, show improved behaviors and improved completion of components of the dental exam compared to their previous routine dental visit.

  3. To evaluate provider perceptions of the behavior and cooperation of children using medical play before dental exam visits compared to dental exam visits without medical play.

  4. To evaluate caregiver perceptions of the behavior and cooperation of children using medical play before dental exam visits compared to dental exam visits without medical play.

  5. To evaluate patient perceptions of the dental exam, visit when medical play is used in comparison to dental exam visits without medical play.

The hypotheses are as follows:
  1. Subjects will have increased positive behaviors and improved cooperation during dental exam visits when medical play is utilized beforehand.

  2. Providers will report improved behavior and cooperation from patients when medical play is utilized beforehand.

  3. Parents will report improved behavior and cooperation from their children and report greater satisfaction with the dental visit when medical play is utilized beforehand.

  4. Patients will report experiencing less anxiety, via the Modified Child Dental Anxiety Scale - Faces Version (MCDAS-f) after appointments in which medical play is utilized.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Medical Play
  • Behavioral: Routine Play
N/A

Detailed Description

The purpose of this study is to investigate the efficacy of medical play to improve the behaviors and cooperation of patients during routine dental exam visits at Children's Hospital Colorado Dental Center through a prospective, randomized controlled trial. The specific aims of this study are to: (1) evaluate differences in behaviors and cooperation levels of subjects utilizing medical play during routine dental exam visits in comparison to those undergoing a routine dental exam visit without use of medical play; (2) evaluate whether subjects who have a dental exam visit, with or without use of medical play, show improved behaviors and improved completion of components of the dental exam compared to their previous routine dental visit; (3) evaluate provider perceptions of the behavior and cooperation of children using medical play during dental exam visits compared to dental exam visits without medical play; (4) evaluate caregiver perceptions of the behavior and cooperation of children using medical play during dental exam visits compared to dental exam visits without medical play; and (5) evaluate patient perceptions of the dental exam visit when medical play is used in comparison to dental exam visits without medical play. To investigate these specific aims, this study will involve recruiting up to 100 neurotypical patients, ages 5-10 years old, who will be seen for their dental exam visits who were previously identified by providers using the Frankl Behavior Rating Scale as Frankl 1 and Frankl 2. Subjects meeting including criteria were screened and offered participating in the study using a telephonic script. Patients agreeing for participation were screened for inclusion and exclusion criteria when they report for routine dental exam and cleaning using pre-screening consent script. Study information, patient rights including voluntary participation and withdrawal of consent without consequences will be provided and informed consent or assent will be collected. The recruited subjects will be randomly divided into two groups so that one group of participants will engage in medical play before the dental exam visit and the other group will be engaged to routine play (coloring exercise) before their dental exam visit. The provider will be blinded to whether the intervention (medical or routine play) before the dental exam visit. The caregivers will complete Dental Behavior Assessment survey before while post-visit survey after the visit to help assess their perceptions of their child's behaviors before and after the visit, respectively. The subjects will also rate their perceived well-being before and after the dental visit using the Modified Child Dental Anxiety Scale - Faces Version. The provider will record patient behavior using a Frankl behavior rating scale and levels of cooperation (which components of the dental exam were completed without coaxing beyond two minutes).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Prospective, randomized clinical controlled trialProspective, randomized clinical controlled trial
Masking:
Double (Participant, Care Provider)
Masking Description:
The dental providers and study subjects will be blinded to the intervention: medical or routine play
Primary Purpose:
Treatment
Official Title:
The Impact of Medical Play in the Dental Clinic Setting on the Cooperation of Neurotypical Patients at Children's Hospital Colorado Dental Center
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2025
Anticipated Study Completion Date :
Oct 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Medical Play Intervention

This group of participants will be engaged in medical play before the dental exam visit.

Behavioral: Medical Play
Study subject will be engage in the medical play.

Placebo Comparator: Routine Play Intervention

This group of participants be engaged in routine play (coloring exercise) before the dental exam visit.

Behavioral: Routine Play
Study subject will be engage in the routine play (coloring exercise).

Outcome Measures

Primary Outcome Measures

  1. Behavior as measured by Frankl score [baseline (post-intervention)]

    This outcome will evaluate differences in behaviors and cooperation levels of subjects engaged in medical play during routine dental exam visits in comparison to those engaged in routine play before their dental exam visit. The subject's behaviors categorized according to the Frankl score which is a standardized ordinal scale to categorize patient behaviors in the dental clinic setting. This score will be determined at the end of the dental visit by the dental provider and compared to the previous routine dental visit for the same subject. Frankl Behavior Rating Scale is between 1-4 and the scoring is as follows: 1 = definitely negative, 2 = negative, 3 = positive, and 4 = definitely positive.

  2. Completion of Components of dental examination [baseline (post-intervention)]

    This outcome will evaluate whether subjects who have a dental exam visit, with medical or routine play, show completion of components of the dental exam compared to their previous routine dental visit. The subject's level of cooperation which will be determined by the number of procedures completed during the routine dental check-up visit which will consist of (1) a dental cleaning (rubber cup or toothbrush prophylaxis), (2) a dental examination (completed with mouth mirror and explorer), and (3) a fluoride varnish application. The number of procedures completed with or without difficulty will be compared to those completed at a previous routine dental visit.

Secondary Outcome Measures

  1. Pre-intervention parental perceptions about their child's behavior [baseline (pre-intervention), post-intervention (immediately after dental visit)]

    My child appears worried during dental visits. My child initially refuses to enter the room. My child initially refuses to sit on the dental chair. My child sits in a chair other than the dental chair or on the ground, or stands, during visits. My child appears anxious about the dental provider brushing his/her teeth. My child will not easily cooperate for a regular dental cleaning. The dental provider is only able to use the regular toothbrush and cannot use the electrical cleaning brush for my child's teeth during the dental visit. My child appears worried about the dentist using the dental mirror to check his/her teeth. The dental provider cannot use the dental mirror and has to look at the teeth directly. The dental provider is not able to use a dental explorer to check my child's teeth. My child needs frequent breaks during dental visits. My child will not allow the dental provider to apply fluoride varnish on his/her teeth.

  2. Patient perception before and after dental visit [baseline (pre-intervention), post-intervention (immediately after dental visit)]

    Provided by Modified Child Dental Anxiety Scale - Faces Version (MCDAS-f). 5 different depictions of faces ranging from very worried to worried are included in the options. Children will point or circle how they feel about the following three questions: How do you feel about going to visit the dentist? How do you feel about having your teeth looked at? How do you feel about having your teeth cleaned and polished? 5 options include: relaxed/not worried very slightly worried fairly worried worried a lot very worried

  3. Post-intervention parental perceptions about their child's behavior [baseline (pre-intervention), post-intervention (immediately after dental visit)]

    A Post visit parent survey will include 3 questions: Do you feel your child's behavior improved today compared to past dental visits? Will be evaluated as: 0. no change. 1. little improvement. 2. Improved. 3. significant improvement. or 4. not sure Do you feel that the intervention/session before dental exam was helpful for your child's behavior and cooperation at today's visit? Will be evaluated as: 0. not helpful. 1. little helpful. 2. helpful. 3. significantly helpful. or 4. not sure Would you want to use the same intervention/session for your child before future dental visits? Will be evaluated as 0.never. 1. maybe. 2. yes. 3. not sure.

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Previously identified as Frankl 1 or Frankl 2 per the electronic dental record during dental exam visits (Epic)

  • Child subject is neurotypical

  • Patient of record at Children's Hospital Colorado Dental Center

  • Child subject is 5-10 years of age

  • Caregiver must be the child's legal guardian

Exclusion Criteria:
  • Previously identified as Frankl 3 or Frankl 4 per the electronic dental record during dental exam visits (Epic)

  • Children who have not previously received care at the Children's Hospital Colorado Dental Center

  • Children that have a diagnosis of Autism or other neurologically atypical diagnosis

  • Children not in the age range of 5-10 years

  • Adult in attendance to dental visit with child is not the legal guardian

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital of Colorado Health Pavilion-Dental Clinic Aurora Colorado United States 80011

Sponsors and Collaborators

  • University of Colorado, Denver

Investigators

  • Principal Investigator: Chaitanya P Puranik, BDS,MS,PhD, University of Colorado - Anschutz Medical Campus

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT05571423
Other Study ID Numbers:
  • 22-1302
First Posted:
Oct 7, 2022
Last Update Posted:
Oct 7, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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 Oct 7, 2022