Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06435208

Impact of Subgingival Instrumentation on Psychological Distress and Mental Health Status in Bruxers With Periodontitis

Bruxism is a non-functional repetitive jaw-muscle activity characterized by grinding or clenching the teeth. Bruxism, characterized by the involuntary grinding or clenching of teeth, is a prevalent parafunctional habit affecting individuals of all ages. Stress, anxiety, and depression are the psychological factors most commonly associated with the presence of bruxism.

Recruiting

Interested in participating?

Request Info

Key information

Age range

30 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Post Graduate Institute of Dental Sciences

Rohtak, Haryana, 124001, India

Location status: Recruiting

Location contact

RAJINDER KR SHARMA, MDS

CONTACT

[email protected]

9416358222

About this study

Bruxism, characterized by the involuntary grinding or clenching of teeth, is a prevalent parafunctional habit affecting individuals of all ages. Although the etiology is not known exactly, it has been suggested that bruxism is a multifactorial disorder. Periodontitis, a prevalent inflammatory condition affecting the periodontium, has been linked to bruxism in several studies. The coexistence of bruxism and periodontitis poses unique challenges in clinical management of periodontitis. Also, as periodontitis became chronic, the occurrence of depression increased. Stress, anxiety, and depression are the psychological factors most commonly associated with the presence of bruxism. Therefore, this study aims to investigate impact of subgingival instrumentation on psychological distress and mental health status in bruxers with periodontitis.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Systemically healthy patients
  • Patient having periodontitis with bruxism
  • Age between 30-50 years

Exclusion criteria

  • History of mental health disorder
  • History of systemic disease
  • History of drugs having the potential impact on periodontal status like phenytoin, cyclosporin, calcium-channel blockers or antidepressant drugs
  • Pregnant or lactating females

Treatment and study plan

Subgingival instrumentation

Other

All the participants will undergo scaling and root planning with hand scalers, curettes and ultrasonic scaler.

Primary outcomes

  1. Psychological distress

    Time frame: BASELINE,2 MONTHS ,3 MONTHS

    Assessment of psychological distress will be done by using Kessler Psychological distress(K10)

  2. Mental Health Status

    Time frame: Baseline, 2 months, 3 months

    Assessment of mental health status will be done by using mental health inventory 38

Secondary outcomes

  1. periodontal parameter

    Time frame: Baseline, 2 month, 3 month

    periodontal probing depth

  2. periodontal inflammation

    Time frame: Baseline, 2 month, 3 month

    bleeding on probing

Study contacts

Contact information is provided by the study sponsor or research team.

Priyanka Chandela, BDS

CONTACT

[email protected]

+917027019277

RAJINDER KR SHARMA, MDS

CONTACT

[email protected]

9416358222

Sponsors and collaborators

Lead sponsor

Postgraduate Institute of Dental Sciences Rohtak

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
May 30, 2024
Registry last updated
Jul 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.