Oral Status and Care Needs of People Aged 90 and Over (PAQUIDENT25)

August 26, 2019 updated by: University Hospital, Bordeaux

Oral Status and Care Needs of People Aged 90 and Over in Gironde and Dordogne

This study will help describe the state of oral health of very old people (over 90).

Study Overview

Status

Completed

Conditions

Detailed Description

In 2011, according to the French National Institute for Statistics and Economic Research, people aged 85 and over accounted for about 3% of the total population. This proportion will increase sharply due to longer life expectancy on the baby boom generation and is expected to reach 7.5% of the total population in 2050.

This very old population has specific health, related to the presence of co-morbidities and co-medications, but also to a frequent state of dependence.

These general health problems and their treatment can create or accentuate oral problems or complicate their management. Thus, very old people are more likely to have some oral diseases although there is no epidemiological data in France. Conversely, oral problems can have repercussions in terms of quality of life, social relations and nutrition, and are factors of risk or aggravating actual or potential systemic disorders.

This very elderly population is therefore likely to present new challenges of dental care that it is important to document.

Study Type

Observational

Enrollment (Actual)

180

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

90 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

This is an ancillary study of the PAQUID cohort, of a cross-sectional nature, descriptive in a representative sample of very elderly people (≥90 years) in the Gironde and Dordogne, monocentric, with home collection.

Description

Inclusion Criteria:

  • Patients over 90 years old
  • Follow-up in 2013-2014 as part of the PAQUID cohort
  • Participation Agreement

Exclusion Criteria:

  • Inability to give informed consent and refusal of legal guardian.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
State of the mouth and teeth
Time Frame: Inclusion visit
Number of decayed, absent and closed teeth
Inclusion visit
Masticatory ability
Time Frame: Inclusion visit
Number of functional units
Inclusion visit
Root caries index
Time Frame: Inclusion visit

Root caries index (RCI) - RCI is based on the requirement that gingival recession must occur before root caries surface lesion begin, therefore only teeth with gum recession are examined.

  • 4 surfaces of root are examined (mesial, distal, lingual, and buccal or labial)
  • A judgment of no gum recession is made if CEJ (cement enamel junction) cannot be visualized.

The root caries index is calculated for an individual using the formula

• RCI= (R-D) +(R-F) x 100 (R-D) +(R-F) +(R-N) R-N =Recession present surface normal or sound R-D =Recession present with decay root surface R-F= Recession present with a filled root surface.

Inclusion visit
Hygiene index
Time Frame: Inclusion visit
Hygiene index (OHI-S, Simplified Oral Hygiene Index ; from 0 to 3)
Inclusion visit
Oral pain
Time Frame: Inclusion visit
Presence of oral pain yes/no
Inclusion visit
Oral lesions
Time Frame: Inclusion visit
Presence and nature of oral lesions according to the International Classification of Diseases applied to odontology and stomatology of the World Health Organization
Inclusion visit
Hyposalivation / xerostomia
Time Frame: Inclusion visit
Presence of hyposalivation / xerostomia (Xerostomia Inventory, XI, 11 items questionary)
Inclusion visit

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Elise ARRIVE, Dr, University Hospital, Bordeaux

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 11, 2014

Primary Completion (Actual)

December 5, 2014

Study Completion (Actual)

December 5, 2014

Study Registration Dates

First Submitted

August 12, 2019

First Submitted That Met QC Criteria

August 21, 2019

First Posted (Actual)

August 22, 2019

Study Record Updates

Last Update Posted (Actual)

August 28, 2019

Last Update Submitted That Met QC Criteria

August 26, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • CHU BX 2013/04

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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