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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03190512
Other study ID # 14-KAEK-218
Secondary ID
Status Completed
Phase N/A
First received June 12, 2017
Last updated June 15, 2017
Start date May 4, 2015
Est. completion date September 1, 2016

Study information

Verified date June 2017
Source Tokat Gaziosmanpasa University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is a relationship between depression and periodontal disease. This relationship may be double-sided. A psychological state such as anxiety, depression, body image, and self-esteem may be affected from the symptoms of periodontal disease.


Description:

Background: Depression is a multi-factorial disease characterized by a variety of symptoms. Psychiatric disorders seem to be more prone to periodontitis compared to patients without psychiatric disorders. However periodontal disease and depression can be considered bidirectional risk factors. Periodontal disease can also be an effect on depression. The aim of this randomized controlled clinical study is to determine the effect of non-surgical mechanical periodontal treatment on psychological state.

Material and methods: The study population consisted of 184 depressed patients with non-treated periodontal diseases. Two randomized group is formed from these patients. Immediately periodontal treatment (test group, n = 92) and delayed periodontal treatment (control group, n = 92). Clinical periodontal and psychological measures were performed at baseline and 6th weeks on control and test group.


Recruitment information / eligibility

Status Completed
Enrollment 184
Est. completion date September 1, 2016
Est. primary completion date March 31, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- the presence of periodontal diseases,

- the presence of diagnosed minor depression

- being under maintenance therapy regarding the depression

Exclusion Criteria:

- any hormonal condition such as pregnancy or lactation

- received any periodontal treatment within six months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Psychological measurements
Four questionnaire tests for depression, body image, self-esteem, and anxiety was performed baseline and after 6 weeks.

Locations

Country Name City State
Turkey Gaziosmanpasa University Tokat

Sponsors (1)

Lead Sponsor Collaborator
Ozge Gokturk

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Depression level The changes in depression level within 6 weeks. Depression level was determined using the Beck Depression Inventory. Baseline and after 6 weeks
Secondary Body image level The changes in body image level within 6 weeks. Body image level was determined using the Body Cathexis Scale. Baseline and after 6 weeks
Secondary Anxiety level The changes in anxiety level within 6 weeks. Anxiety level was determined using the Beck Anxiety Inventory. Baseline and after 6 weeks
Secondary Self-esteem level The changes in self-esteem level within 6 weeks. Self-esteem level was determined using the Rosenberg Self-Esteem Scale. Baseline and after 6 weeks
Secondary Probing pocket depth The changes in probing pocket depth after periodontal treatment.Probing pocket depth was measured for determining severity of disease and clinic outcome. Baseline and after 6 weeks
Secondary Clinical attachment level The changes in clinical attachment level after periodontal treatment. Clinical attachment level was measured for determining severity of disease and clinic outcome. Baseline and after 6 weeks
Secondary Gingival index The changes in gingival index level after periodontal treatment. Clinical attachment level was measured for determining severity of disease and clinic outcome. Baseline and after 6 weeks
Secondary Plaque index The changes in plaque index after periodontal treatment. Plaque index was recorded for determining and classifying oral hygiene status. Baseline and after 6 weeks
Secondary Bleeding on probing The changes in bleeding on probing after periodontal treatment. Bleeding on probing was recorded for classifying and evaluating (apically) gingival inflammation. Baseline and after 6 weeks
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