A Telephone-based Case-management Intervention for Caries Prevention in Children With Severe Early Childhood Caries
Despite improvements in oral health among children, children living in areas characterized by low socio-economic status still have a significant disease burden with regard to dental caries. Special efforts to prevent disease development in this group of children have been unsuccessful. Small children with extensive treatment needs often have limited abilities to cooperate and to provide quality dental care in this patient group, general aneaethesia (GA) may often be the treatment modality of choice. Preschool children treated under general anesthesia have significantly higher caries prevalence (deft and defs), apical parodontitis and infection due to pulpal necrosis. They also have significantly more emergency visits and previous use of treatment under sedation.
This study aim to test the hypothesis, that a telephone based case management intervention for children with severe early childhood caries can prevent further caries development in preschool children who are treated under general anesthesia for severe early childhood caries.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Consecutive children (n=130) who are referred to the departments of pediatric dentistry at Eastman Dental Institute, Public Dental Service and Dental Medicine, Karolinska Institutet, who fulfill inclusion criteria are invited to participate in the study. This is done during the visits preceding the anesthetic evaluation of the patient. Parents will be given written information about the study. During the last visit preceding the GA, a contact is established between dental health coach and family. During this visit the aim of the project is explained and an agreement is signed and informed consent is obtained from the parents only (the parents are the target for this intervention, it is they who perform the preventive oral health measures and supports the child). During this interview, the parents will also answer a structured interview measuring level of self-efficacy and well as their thoughts on dental health care as well as why the situation has occurred. After the initial interview patients are assigned to either intervention group (dental health coach group) or to a control group.
The dental healthcoach will keep in close contact with the intervention group, and by telephone based support provide information, support parental self-efficacy, motivate the family to keep preventive measures that have been individually agreed on, motivate parents to keep preventive appointments and to provide tools for caries prevention.
A follow-up visit is scheduled after 1 year. Parents who decline participation in the program will receive treatment as usual and will be followed for 1 year.
Patients in the control group will receive treatment as usual. This means recall visits to the dental clinic within 3 months after the procedure, reinforcing the individually tailored preventive program. Recall visits after that are scheduled based on treatment needs. A follow-up visit is scheduled after 1 year.
Caries will be diagnosed at baseline ( during GA) and progression will be monitored according to ICDAS after 12 and 24 months. Plaque and gingivitis will be registered.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Huddinge
-
Stockholm, Huddinge, Sweden, 141 04
- Karolinska Institutet
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Pre-school children < 6 years of age
- Severe childhood caries
- treated under general anesthesia in Stockholm County Council during a one year period.
Exclusion Criteria:
- Medically compromised children
- Children with learning disabilities
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dental health coaches
Telephone-based case-management intervention.
Contact with families every 2 weeks during one year.
Including motivational interviewing, support for dental preventive measures at home, answer questions, care coordination) + conventional protocol (Fluoride prevention program)
|
Regular Telephone support delivered by Health coaches
|
|
No Intervention: Control group
Conventional protocol (Fluoride prevention program) and follow-up as usual
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in New carious lesion (decayed surfaces and decayed teeth) at 12 and 24 months
Time Frame: 12 months, 24 months
|
decayed surfaces (dmfs) and decayed teeth (dmft)
|
12 months, 24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dental attendance
Time Frame: 12 months
|
number of visits to dental health care during the observation period, number of unscheduled appointments, number of missed and cancelled appointments
|
12 months
|
|
oral health related quality of life
Time Frame: 12 months
|
Validated scale OHRQoL, subscales FIS and P-CPQ will be used
|
12 months
|
|
Dental Anxiety among parents
Time Frame: 12 months
|
Dental Anxiety Scale, DAS
|
12 months
|
|
Parental Stress
Time Frame: 12 months
|
The Swedish Parenthood Stress Questionnaire - SPSQ
|
12 months
|
|
Dental beliefs among parents
Time Frame: 12 months
|
Swedish version of the revised Dental Beliefs Survey (DBS-R)
|
12 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dental health coaches' experiences of their role
Time Frame: 18 months
|
Questioners and focus groups will be used to understand the experience of the health coach in order to refine the intervention in future projects
|
18 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Göran Dahllöf, Professor, Karolinska Institutet
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Dnr 1-314/2013 SOF, KI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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