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Oral Hygiene Self-efficacy in Patients With Grief — OHGRIEF  

Grief Clinical Trial

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

Clinical Trial Summary

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

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03286647
Study type Interventional
Source University of Sao Paulo General Hospital
Contact Francisco Lotufo-Neto, PhD
Phone (05511) 2661-6988
Email franciscolotufo@gmail.com
Status Not yet recruiting
Phase N/A
Start date October 5, 2017
Completion date October 5, 2018
View Details
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