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Oral Hygiene Self-efficacy in Patients With Grief

Evaluation of Oral Hygiene Self-efficacy in Patients With Grief: a Short-term Randomized Controlled Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03286647
Acronym
OHGRIEF
Enrollment
90
Registered
2017-09-18
Start date
2017-10-05
Completion date
2018-10-05
Last updated
2017-09-18

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

Conditions

Grief

Keywords

grief, periodontal disease

Brief summary

to investigate the effect of oral hygiene self-efficacy in patients with grief (G) and complicated grief (CG)

Detailed description

Aim: to investigate the effect of oral hygiene self-efficacy in patients with grief (G) and complicated grief (CG). Study design: randomized controlled trial. Setting: Institute of Psychiatry-FMUSP (Ipq-FMUSP). Subjects: cases: patients seeking for treatment or under treatment for CG (Group 1), and patients with normal grief (Group 2). Controls: Hospital staff at the HC-FMUSP or volunteers from a list of other studies conducted at the Ipq-FMUSP (Group 3). Method. Psychiatric evaluation: Structured Clinical Interview (SCID), Texas Revised Inventory of Grief (TRIG) and clinical interview. Intervention: instruction of oral hygiene. Dental evaluation: probing depth, clinical attachment level, bleeding on probing, and frequency of plaque at six sites per tooth. Procedures: all participants will complete the psychiatry and dental evaluation at baseline. The bleeding on probing and frequency of plaque will be recorded at baseline, once a week (1 month follow-up) and at 3 months. The probing depth and clinical attachment level will be recorded at baseline and at 3 months. After 3 months, the patients will be referred for dental treatment.

Interventions

the participants will receive instructions to perform a satisfatory oral hygiene

Sponsors

University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of grief or complicated grief * Informed consent signature

Exclusion criteria

* Patients with severe major depressive disorder at risk for suicide; * Substance abuse or dependence, * Psychotic disorders * Systemic alteration that precludes periodontal clinical examination

Design outcomes

Primary

MeasureTime frameDescription
Frequency of dental plaqueChange from baseline, 1 and 3 months after oral hygiene instructionfrequency of dental plaque at 6 sites per tooth

Secondary

MeasureTime frameDescription
probing depthChange from baseline and 3 months after oral hygiene instructiondistance of gingival margin to probe tip
clinical attachment levelChange from baseline and 3 months after oral hygiene instructiondistance of cemento-enamel junction to probe tip
Bleeding on probingChange from baseline, 1 and 3 months after oral hygiene instructionfrequency of bleeding on probing at 6 sites per tooth

Countries

Brazil

Contacts

Primary ContactFrancisco Lotufo-Neto, PhD
franciscolotufo@gmail.com(05511) 2661-6988

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026