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Supervised versus non-supervised implementation of an oral health care guideline in (residential) care homes: A cluster randomized controlled clinical trial.

Supervised versus non-supervised implementation of an oral health care guideline in (residential) care homes: A cluster randomized controlled clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29576
Enrollment
360
Registered
2010-08-13
Start date
2009-01-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral health care, Oral hygiene, Oral health, Care Homes, nursing homes, oral health guideline, older people.

Interventions

The intervention consists of supervised implementation of the guideline “Oral health care in (residential) care homes for elderly people” and the daily oral health care protocol derived from the guide
2. A 2-hour lecture and in total 3 hours of practical education for the WOO’s. The education, presented by the dental hygienist, regards the theoretical and practical essentials of the guideline. The
3. A 1.5-hour theoretical and executive education session at each ward, presented by the WOO, for all ward nurses and nurse aides. This education session is scheduled after the baseline data collectio

Sponsors

Birkhoven Zorggoed, Radboud University Nijmegen Medical Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: To participate in the study, a resident should: 1. Supply a written informed consent, undersigned by himself or his legal representative; 2. Have teeth and/or partial or complete dentures; 3. Have the cognitive and physical condition required for undergoing an oral examination; 4. Be residing in the institution during the entire 6-months period presumably.

Exclusion criteria

Exclusion criteria: Residents are excluded when in day-care, in short-term residency, in coma, in palliative care or terminally ill, using a denture adhesive, expressing verbal or physical resistiveness before or during an oral examination.

Design outcomes

Primary

MeasureTime frame
Primary outcome variable is the oral hygiene level of the participating residents.

Secondary

MeasureTime frame
To determine the stimulating or inhibiting factors of the implementation project and the nurses’ and nurse aides’ compliance and perceived barriers, a process evaluation is carried out.

Contacts

Public ContactG.J. Putten, van der

Birkstraat 200

gjvdputten@hetnet.nl+31 (0)33 4600500

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)