Oral Hygiene Intervention Pilot Study

Dental Caries Clinical Trial

Official title:

Iowa Nursing Facility Oral Hygiene Intervention: A Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02668809
• Other study ID #: INFOH
• Status: Completed
• Phase: N/A
• Start date: June 2014
• Est. completion date: June 2018

Study information

• Verified date: August 2018
• Source: University of Iowa
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main goals of this pilot study are to develop a nursing home-customized oral hygiene protocol, intended to be delivered primarily by dental hygienists and primary care providers, and to identify potential obstacles and barriers to overcome in designing a subsequent definitive study on the same topic.

Description:

For the purposes of this pilot study, a convenience sample from six (6) to twelve (12) nursing facilities will be selected and randomly assigned into three groups: Experimental group 1 (educational program only, performed by a dental hygienist); Experimental group 2 (educational program plus 1% chlorhexidine varnish application monthly for the residents); Control group (current oral hygiene practice). Several objective and subjective oral and general health measures will be observed before and after the interventions to evaluate the impact of the interventions on the oral and general health of the residents and also of the direct care workers.

Assigned personnel in each nursing facility (NF) will be interviewed to identify possible barriers to provide oral care. Each interview will take one hour, approximately.

All residents that agree to participate will be interviewed and have an oral examination and dental plaque sample collection by the investigators. Each appointment will take 30 minutes. The subject's health record in the nursing facilities will be abstracted for medical information (date of birth, sex, race, source of payment for NF residency, comorbid conditions, weight, height, medications, number of febrile days, and x-ray documented pneumonia episodes).

After that, the educational program will be delivered in a standardized fashion for all NF in the "educational program only group": 1) Cognitively capable residents will receive instruction on how to perform their own oral hygiene accordingly to their own needs (approximately 15 minutes); and 2) Direct care workers will receive instruction on how to perform oral hygiene for dependent residents or supervise the oral hygiene routines of independent patients (01 hour session). For both 1) and 2) above, dental hygienists will provide a short, standardized presentation and hands-on demonstration. In addition, the dental hygienist will provide in situ oral care (plaque and gingival bleeding index assessment, microbiological sampling and toothbrushing with chlorhexidine mouth rinse) on a bi-weekly basis during the study period (15 minute each appointment) .

The "educational program plus 1% chlorhexidine varnish application group" will receive the educational program described above. In addition, residents who need supervision or are unable to perform oral hygiene procedures will receive 1% chlorhexidine varnish application monthly by the dental hygienist. No additional time commitment will be necessary.The direct care workers will NOT receive any varnish.

The control group will not receive any intervention through this protocol during the formal study period, but if the initial results are promising they will be invited after the formal study period to receive the educational program.

After a six month period from the initial examination,all residents and direct care workers that agree to participate will be interviewed and have an oral examination and dental plaque sample collection by the investigators again. Each appointment will take 30 minutes.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 81
• Est. completion date: June 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years to 120 Years

Eligibility

Inclusion Criteria:

• be a resident or primary care worker in one of the following nursing homes: Linn Manor Care Center Simpson Memorial Home, Inc., Wilton Retirement Community, All-American Care of Muscatine, Pioneer Park of Lone Tree, Colonial Manor of the Columbus Community, Sunrise Terrace Nursing and Rehabilitation Center Parkview Home-Wayland.

• age 21-120

Exclusion criteria:

Only those who do not sign the consent form will be excluded

Exclusion Criteria:

• not a resident or primary care worker in one of the above listed retirement homes

• age less than 21 or greater than 110

Related Conditions & MeSH terms

• Dental Caries
• Gingivitis

Intervention

Other:
• oral health assessment
A baseline oral health assessment of both residents and direct care workers will be conducted before interventions are initiated. Data will be entered directly into a spreadsheet format using the chairside software program to be developed as part of this proposal.
• Questionnaires
Age, sex, race, nutrition (mini-nutri), quality of life (SF-36), OHIP-14, GOHAI, sources of payment for the NF residency, comorbid conditions (e.g., constipation, arthritis), weight, medications, cognitive status (mini-mental) , dry mouth sensation, x-ray documented pneumonia;
• Clinical Exam
Dentate status, dental/denture plaque index, DMFS (including root surfaces), gingival bleeding index, plaque index, presence of oral lesions, verification of mouth dryness;
• Microbiological sampling
Samples will be collected by swabbing patients intra-oral tissues. Samples will be separately collected from dentures and oral tissues for edentulous patients, also using swabs. All samples will be suspended in saline solution.
• Monitoring Adherence
Adherence to the protocol will be evaluated through unannounced observations at the NF by study personnel twice per month. Adherence is determined by direct observation of the DCW administering the intervention.
• Varnish application
1% chlorhexidine varnish application group" will receive the educational program described above. In addition, residents who need supervision or are unable to perform oral hygiene procedures will receive 1% chlorhexidine varnish application monthly by the dental hygienist. No additional time commitment will be necessary.The direct care workers will NOT receive any varnish.
• Consent
Both the residents and primary care workers will be asked to participate on the study, and the investigators will provide information and collect signed informed consents primarily during two in person visits to each nursing facilities.
• Educational Program
Cognitively capable residents will receive instruction on how to perform their own oral hygiene accordingly to their own needs; and 2) Direct care workers will receive instruction on how to perform oral hygiene for dependent residents or supervise the oral hygiene routines of independent patients. For both 1) and 2) above, dental hygienists will provide a short, standardized presentation and hands-on demonstration.

Locations

Country	Name	City	State
United States	UIowa	Iowa City	Iowa

Sponsors (3)

Lead Sponsor	Collaborator
Leonardo Marchini	Delta Dental of Iowa, Ivoclar Vivadent AG

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Plaque index	Percentage reflecting the proportion of teeth surfaces covered by plaque, assessed by intra-oral exam.	6 months
Primary	Denture plaque index	Index reflecting the proportion of denture surfaces covered by plaque, assessed by denture exam.	6 months
Primary	Gingival bleeding index	Index reflecting the proportion of gingival areas Bleeding on probing, assessed by intra-oral exam.	6 months
Primary	Decayed, missing or filled surfaces (DMFS) index	Index reflecting the number of decayed, missing or filled teeth surfaces, assessed by intra-oral exam.	6 months
Primary	Total microbial count	Numbers of viable bacteria per swab will be determined following sector counting and analysis following standard spiral plating methodology	6 months
Primary	Isolation and enumeration of our target species: Porphyromonas gingivalis, Prevotella intermedia, Methicillin-Resistant Staphylococcus aureus (MRSA), Pseudomonas aeruginosa, Actinomyces spp., Fusobacterium nucleatum, and Candida albicans.	Plates will be counted following standard incubation times for each group of organisms and numbers of viable bacteria per swab will be determined following sector counting and analysis following standard spiral plating methodology.	6 months
Secondary	Assessment of residents cognitive status using Mini Cog test	Mini-Cog test is a 3-minute instrument to screen for cognitive impairment in older adults in the primary care setting.The instruments will be applied at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of cognitively sound participants quality of life using SF-36 questionnaire	The Short Form (36) Health Survey is a 36-item, patient-reported survey about quality of life. The instruments will be applied at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of cognitively sound participants oral health-related quality of life using OHIP 14	Oral Health Impact Profile 14 questions questionnaire (OHIP-14) is a validated, commonly used, comprehensive questionnaire about oral-health related quality of life. The instruments will be applied at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of cognitively sound geriatric participants oral health-related quality of life using GOHAI	The Geriatric Oral Health Assessment Index (GOHAI) is a validated, widely used questionnaire developed to assess oral health perceptions among geriatric populations.The instruments will be applied at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of participants nutritional status using Mini Nutritional Assessment Short Form	The Mini Nutritional Assessment Short Form is a short questionnaire that also considers the BMI (weight in kg/height in m2) and provides an estimate of an individuals nutritional state. The instruments will be applied at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of number of events of x-ray documented pneumonia	X-ray documented pneumonia events are assessed through medical records at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of number of febrile days	Number of febrile days are assessed through medical records at baseline and end of the experiment protocol.	6 months
Secondary	Assessment of dry mouth sensation	Participants are asked about feeling their mouth dry at baseline and by the end of the experimental protocol	6 months
Secondary	Assessment of the presence of oral lesions	Presence of oral lesions was assessed by clinical exam at baseline and by the end of the experimental protocol	6 months