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Intervention Study of Oral Health Education Programs Directed to Adolescents

G

Göteborg University

Status

Completed

Conditions

Periodontal Infection
Gingivitis

Treatments

Behavioral: Patient centered oral health education
Behavioral: Standard educational intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02906098
kajsaha

Details and patient eligibility

About

This study evaluates behavioral interventions to increase adolescent's motivation for self performed periodontal infection control, by means of adequate oral hygiene. Study subjects will be allocated to test and control group where the test will be subjected to an individually tailored oral health education program, based on cognitive- behavioral theory and principles, and the control to standard educational intervention.

Full description

The prevalence of chronic periodontitis is about 40% among the Swedish adult population. The key-factor for the prevention of periodontal disease progression is the establishment of periodontal infection control, by means of adequate daily oral hygiene. Hence, a main task for dental professionals is to educate and motivate the patient to such beneficial behavior. A hypothesis for the current study is that patient centered health promotion programs based on cognitive behavioral theory and principles and with a directive communicative approach, i.e. motivational interviewing techniques, add positive and lasting effects to standard educational interventions on self-performed periodontal infection control.

This randomized clinical field study involves 30 professionals (dental hygienists) and about 350 adolescent patients at 16 dental clinics in the Västra Götaland Region, Sweden. The approach in the evaluation is on patient-centered outcomes and health economics.

Enrollment

312 patients

Sex

All

Ages

16 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 16 or 17 years old at inclusion
  • poor oral hygiene conditions (dental plaque and/or marginal gingival bleeding at >50% of tooth surfaces) at the time of examination and thus considered to be at increased risk for oral/periodontal disease progression.

Exclusion criteria

  • compromised medical or mental conditions that may requiring special care.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

312 participants in 2 patient groups

Patient centered oral health education
Experimental group
Description:
The program is based on cognitive behavioral theory and principles. Hence, the intervention is adapted to each individual's problem, capacity and goals were the dental hygienist use motivational interviewing skills in communication and act as a guiding resource during the process of behavioral change. The program follows a specific structure including components such as formulation of personal goals, continuous self-monitoring by diary and planning of behavior. The initial intervention phase contain 3 treatment sessions (45-60 min each) during a period of 12 weeks (baseline, 2-3 weeks and 10-12 weeks). Follow up are performed at 6- and 18-months.
Treatment:
Behavioral: Patient centered oral health education
Standard educational intervention
Active Comparator group
Description:
The subjects in the control group receive educational intervention by a dental hygienist in accordance with conventional routines (oral health information and oral hygiene instruction at one or several occasions). Follow up are performed at 6- and 18-months.
Treatment:
Behavioral: Standard educational intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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