search
Back to results

Impact of Periodontal Therapy on Mental Health Parameters (LeakBrainRCT)

Primary Purpose

Periodontitis, Depression

Status
Not yet recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Standard periodontal therapy (steps 1 & 2)
supragingival debridement with anesthesia (step 1)
Sponsored by
Universidad Complutense de Madrid
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

5.3.1. Inclusion criteria: Age greater or equal to 18 years. Patients with moderate or severe major depression, without severe suicide ideation, as characterized by the Patient Health Questionnaire (PHQ)-9 index (values of 9 or greater) and by the Structured Clinical Interview for DSM-5 - (SCID) will be selected. Subjects with periodontitis stages III or IV, according to the 2018 Classification on periodontal and peri-implant diseases (Papapanou et al., 2018). 5.3.2. Exclusion criteria: Pregnant or breastfeeding women. Diabetes mellitus. Chronic conditions: HIV infection, chronic intake of NSAIDs. Comorbidity with other mental disorders: eating disorders, borderline personality disorders, bipolar disorders, schizophrenia and related disorders, and/or any mental serious disease other than major depression. Severe suicide ideation. Smokers of 10 or more cigarettes per day. Patients who had received periodontal treatment for periodontitis in the last year. Presence of necrotizing periodontal diseases. Presence of less than 3 teeth per quadrant. Antibiotic use in the last 6 months prior to the study.

Sites / Locations

  • Faculty of Dentistry, University Complutense of Madrid (UCM)
  • Instituto de Psiquiatría y Salud Mental, Hospital Clínico San Carlos

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Subgingival therapy

Supragingival therapy

Arm Description

Participant will receive standard periodontal treatment consisting of two sessions of supra- and subgingival debridement (steps 1 and 2) under local anesthesia following current guidelines for periodontal therapy in patients with periodontitis (Herrera et al., 2022; Sanz et al., 2020). The use of chlorhexidine (0.12%) and cetylpyridinium chloride (0.05%) mouthwash will be prescribed twice a day for 15 days (Perio-Aid®, Dentaid, Barcelona, Spain). If needed, hopeless teeth might be extracted during this step.

Periodontal treatment consisting of two sessions of supragingival debridement with anesthesia (step 1) and administration of a placebo mouthwash (FluorAid®, Dentaid, Barcelona, Spain), twice a day for 15 days.

Outcomes

Primary Outcome Measures

Hamilton scale (HAM-D17)
Range: 0 to 52. The higher the score, the more severethe depressive symptoms
Hamilton scale (HAM-D17)
Range: 0 to 52. The higher the score, the more severethe depressive symptoms
Hamilton scale (HAM-D17)
Range: 0 to 52. The higher the score, the more severethe depressive symptoms

Secondary Outcome Measures

Childhood Trauma Questionnaire short form (CTQ-SF)
Range: 25 to 125. A higherscore means more (and worst) traumatic experience
Childhood Trauma Questionnaire short form (CTQ-SF)
Range: 25 to 125. A higherscore means more (and worst) traumatic experience
Childhood Trauma Questionnaire short form (CTQ-SF)
Range: 25 to 125. A higherscore means more (and worst) traumatic experience
UCLA Loneliness Scale (Spanish version)
Range: 20 to 80. Higher scores indicatehigher levels of loneliness
UCLA Loneliness Scale (Spanish version)
Range: 20 to 80. Higher scores indicatehigher levels of loneliness
UCLA Loneliness Scale (Spanish version)
Range: 20 to 80. Higher scores indicatehigher levels of loneliness
The World Health Organization Quality of Life questionnaire (WHOQOL)
Range: o to100. A higher score means better quality of life.
The World Health Organization Quality of Life questionnaire (WHOQOL)
Range: o to100. A higher score means better quality of life.
The World Health Organization Quality of Life questionnaire (WHOQOL)
Range: o to100. A higher score means better quality of life.
Beck Depression Inventory (BDI)
Range: 0 to 63. A higher score means more severe-depressive symptomatology
Beck Depression Inventory (BDI)
Range: 0 to 63. A higher score means more severe-depressive symptomatology
Beck Depression Inventory (BDI)
Range: 0 to 63. A higher score means more severe-depressive symptomatology
Centre for Epidemiologic Studies Depression scale [CES-D]
Range: 0 to 60. Higher scores indicate the presence of more severe symptomatology
Centre for Epidemiologic Studies Depression scale [CES-D]
Range: 0 to 60. Higher scores indicate the presence of more severe symptomatology
Centre for Epidemiologic Studies Depression scale [CES-D]
Range: 0 to 60. Higher scores indicate the presence of more severe symptomatology
Global Assessment of Functioning (GAF) Scale
Range: 1 to 100. A higher scoremeans better functioning. A score of 0 means Inadequate information.
Global Assessment of Functioning (GAF) Scale
Range: 1 to 100. A higher scoremeans better functioning. A score of 0 means Inadequate information.
Global Assessment of Functioning (GAF) Scale
Range: 1 to 100. A higher scoremeans better functioning. A score of 0 means Inadequate information.

Full Information

First Posted
July 26, 2023
Last Updated
September 6, 2023
Sponsor
Universidad Complutense de Madrid
Collaborators
Ministerio de Economía y Competitividad, Spain
search

1. Study Identification

Unique Protocol Identification Number
NCT06036472
Brief Title
Impact of Periodontal Therapy on Mental Health Parameters
Acronym
LeakBrainRCT
Official Title
Impact of Periodontal Therapy on Mental Health Parameters in Patients With Major Depression and Periodontitis: a Pilot Randomized Controlled Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidad Complutense de Madrid
Collaborators
Ministerio de Economía y Competitividad, Spain

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Objectives: Primary: To determine the efficacy of periodontal treatment on mental health outcomes in patients with major depression and periodontitis. Secondary: To identify the effect of periodontal treatment on oral, periodontal, and fecal metagenomic microbiomes, and on systemic levels of inflammation (bacterial, viral, and fungal) and their impact on mental health outcomes. Material and method: A 6-month pilot randomized controlled clinical trial is designed. The study will be conducted in patients with moderate or severe DM (Patient Health Questionnaire-9 [PHQ-9] index of 9 or higher) and stage III-IV periodontitis who will be assigned to two different interventions: Test group: standard periodontal treatment consisting of two sessions of supragingival and subgingival debridement (steps 1 and 2) under local anesthesia. Control group: periodontal treatment consisting of two sessions of supragingival debridement (step 1) under local anesthesia. The study will consist of 6 visits: Screening visit (v0) Baseline visit (v1): In the mental health center: patients will receive a structured clinical interview for the DSM-IV (SCID) and the patient will fill out a series of specific scales on a study-specific electronic device [Beck Depression Inventory (BDI); UCLA Loneliness Scale, Center for Epidemiologic Studies Depression scale [CES-D]; Childhood Trauma Questionnaire short form (CTQ-SF); The World Health Organization Quality of Life questionnaire (WHOQOL); Hamilton scale (HAM-D17); Global Assessment of Functioning (GAF) Scale]. At the UCM School of Dentistry: patients will receive a complete periodontal examination (clinical and radiographic). A subgingival microbiological sample, a saliva sample and a blood sample will also be taken. At the participant's home: the stool samples will be deposited by the participants at home in the specific collection vial. Intervention visits (v2-3): Two periodontal treatment sessions (test or control) will be carried out one week apart. Re-evaluation visit (v4): Six weeks after treatment, all periodontal clinical variables will be recorded. Follow-up visits at 3 and 6 months: after periodontal treatment, all the variables recorded at the baseline visit will be taken Statistical analysis: Periodontal treatment (test/control) will be considered as the independent variable and the Hamilton scale (HAM-D17) will be considered the primary response variable. The rest of the variables will be considered as secondary variables. A crude bivariate analysis of comparison of means or proportions will be carried out depending on the nature of the variable. In addition, crude and adjusted regression models will be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontitis, Depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Subgingival therapy
Arm Type
Experimental
Arm Description
Participant will receive standard periodontal treatment consisting of two sessions of supra- and subgingival debridement (steps 1 and 2) under local anesthesia following current guidelines for periodontal therapy in patients with periodontitis (Herrera et al., 2022; Sanz et al., 2020). The use of chlorhexidine (0.12%) and cetylpyridinium chloride (0.05%) mouthwash will be prescribed twice a day for 15 days (Perio-Aid®, Dentaid, Barcelona, Spain). If needed, hopeless teeth might be extracted during this step.
Arm Title
Supragingival therapy
Arm Type
Other
Arm Description
Periodontal treatment consisting of two sessions of supragingival debridement with anesthesia (step 1) and administration of a placebo mouthwash (FluorAid®, Dentaid, Barcelona, Spain), twice a day for 15 days.
Intervention Type
Procedure
Intervention Name(s)
Standard periodontal therapy (steps 1 & 2)
Intervention Description
participant will receive standard periodontal treatment consisting of two sessions of supra- and subgingival debridement (steps 1 and 2) under local anesthesia following current guidelines for periodontal therapy in patients with periodontitis (Herrera et al., 2022; Sanz et al., 2020). The use of chlorhexidine (0.12%) and cetylpyridinium chloride (0.05%) mouthwash will be prescribed twice a day for 15 days (Perio-Aid®, Dentaid, Barcelona, Spain). If needed, hopeless teeth might be extracted during this step.
Intervention Type
Procedure
Intervention Name(s)
supragingival debridement with anesthesia (step 1)
Intervention Description
periodontal treatment consisting of two sessions of supragingival debridement with anesthesia (step 1) and administration of a placebo mouthwash (FluorAid®, Dentaid, Barcelona, Spain), twice a day for 15 days.
Primary Outcome Measure Information:
Title
Hamilton scale (HAM-D17)
Description
Range: 0 to 52. The higher the score, the more severethe depressive symptoms
Time Frame
Baseline
Title
Hamilton scale (HAM-D17)
Description
Range: 0 to 52. The higher the score, the more severethe depressive symptoms
Time Frame
3 months
Title
Hamilton scale (HAM-D17)
Description
Range: 0 to 52. The higher the score, the more severethe depressive symptoms
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Childhood Trauma Questionnaire short form (CTQ-SF)
Description
Range: 25 to 125. A higherscore means more (and worst) traumatic experience
Time Frame
Baseline
Title
Childhood Trauma Questionnaire short form (CTQ-SF)
Description
Range: 25 to 125. A higherscore means more (and worst) traumatic experience
Time Frame
3 months
Title
Childhood Trauma Questionnaire short form (CTQ-SF)
Description
Range: 25 to 125. A higherscore means more (and worst) traumatic experience
Time Frame
6 months
Title
UCLA Loneliness Scale (Spanish version)
Description
Range: 20 to 80. Higher scores indicatehigher levels of loneliness
Time Frame
Baseline
Title
UCLA Loneliness Scale (Spanish version)
Description
Range: 20 to 80. Higher scores indicatehigher levels of loneliness
Time Frame
3 months
Title
UCLA Loneliness Scale (Spanish version)
Description
Range: 20 to 80. Higher scores indicatehigher levels of loneliness
Time Frame
6 months
Title
The World Health Organization Quality of Life questionnaire (WHOQOL)
Description
Range: o to100. A higher score means better quality of life.
Time Frame
Baseline
Title
The World Health Organization Quality of Life questionnaire (WHOQOL)
Description
Range: o to100. A higher score means better quality of life.
Time Frame
3 months
Title
The World Health Organization Quality of Life questionnaire (WHOQOL)
Description
Range: o to100. A higher score means better quality of life.
Time Frame
6 months
Title
Beck Depression Inventory (BDI)
Description
Range: 0 to 63. A higher score means more severe-depressive symptomatology
Time Frame
Baseline
Title
Beck Depression Inventory (BDI)
Description
Range: 0 to 63. A higher score means more severe-depressive symptomatology
Time Frame
3 months
Title
Beck Depression Inventory (BDI)
Description
Range: 0 to 63. A higher score means more severe-depressive symptomatology
Time Frame
6 months
Title
Centre for Epidemiologic Studies Depression scale [CES-D]
Description
Range: 0 to 60. Higher scores indicate the presence of more severe symptomatology
Time Frame
Baseline
Title
Centre for Epidemiologic Studies Depression scale [CES-D]
Description
Range: 0 to 60. Higher scores indicate the presence of more severe symptomatology
Time Frame
3 months
Title
Centre for Epidemiologic Studies Depression scale [CES-D]
Description
Range: 0 to 60. Higher scores indicate the presence of more severe symptomatology
Time Frame
6 months
Title
Global Assessment of Functioning (GAF) Scale
Description
Range: 1 to 100. A higher scoremeans better functioning. A score of 0 means Inadequate information.
Time Frame
Baseline
Title
Global Assessment of Functioning (GAF) Scale
Description
Range: 1 to 100. A higher scoremeans better functioning. A score of 0 means Inadequate information.
Time Frame
3 months
Title
Global Assessment of Functioning (GAF) Scale
Description
Range: 1 to 100. A higher scoremeans better functioning. A score of 0 means Inadequate information.
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Plaque index
Description
presence/absence
Time Frame
Baseline
Title
Plaque index
Description
presence/absence
Time Frame
3 months
Title
Plaque index
Description
presence/absence
Time Frame
6 months
Title
Bleeding on probing
Description
Assessed dichotomously within 15 seconds after probing
Time Frame
Baseline
Title
Bleeding on probing
Description
Assessed dichotomously within 15 seconds after probing
Time Frame
3 months
Title
Bleeding on probing
Description
Assessed dichotomously within 15 seconds after probing
Time Frame
6 months
Title
Suppuration on probing
Description
Assessed dichotomously post-probing
Time Frame
Baseline
Title
Suppuration on probing
Description
Assessed dichotomously post-probing
Time Frame
3 months
Title
Suppuration on probing
Description
Assessed dichotomously post-probing
Time Frame
6 months
Title
Probing depth
Description
Defined as the distance in mm between the bottom of the pocket and the gingival margin
Time Frame
Baseline
Title
Probing depth
Description
Defined as the distance in mm between the bottom of the pocket and the gingival margin
Time Frame
3 months
Title
Probing depth
Description
Defined as the distance in mm between the bottom of the pocket and the gingival margin
Time Frame
6 months
Title
Recession
Description
defined as the distance in mm between the amelocemental boundary and the gingival margin.
Time Frame
Baseline
Title
Recession
Description
defined as the distance in mm between the amelocemental boundary and the gingival margin.
Time Frame
3 months
Title
Recession
Description
defined as the distance in mm between the amelocemental boundary and the gingival margin.
Time Frame
6 months
Title
Number of teeth lost
Time Frame
Baseline
Title
Number of teeth lost
Time Frame
3 months
Title
Number of teeth lost
Time Frame
6 months
Title
Microbiological outcomes
Description
Subgingival biofilm samples will be taken from samples of gingival crevicular fluid. DNA samples will be frozen at -20°C and preserved until further analysis by quantitative polymerase chain reaction (q-PCR) and 16S rRNA sequencing, using the Illumina MiSeq platform
Time Frame
Baseline
Title
Microbiological outcomes
Description
Subgingival biofilm samples will be taken from samples of gingival crevicular fluid. DNA samples will be frozen at -20°C and preserved until further analysis by quantitative polymerase chain reaction (q-PCR) (Marín et al., 2019) and 16S rRNA sequencing, using the Illumina MiSeq platform
Time Frame
3 months
Title
Microbiological outcomes
Description
Subgingival biofilm samples will be taken from samples of gingival crevicular fluid. DNA samples will be frozen at -20°C and preserved until further analysis by quantitative polymerase chain reaction (q-PCR) (Marín et al., 2019) and 16S rRNA sequencing, using the Illumina MiSeq platform
Time Frame
6 months
Title
Plasma levels of inflammatory mediators
Description
Interleukin-1β, Tumor Necrosis Factor-α, prostaglandin-E2, C reactive protein, D-Lactate and intestinal-type fatty acid binding protein 2 [FABP2]), lipopolysaccharide (LPS). matrix metalloproteinase (MMP)-9 levels, S-100B protein levels, quinolinic acid levels, and the ratio between kynurenic and quinolinic acid
Time Frame
Baseline
Title
Plasma levels of inflammatory mediators
Description
Interleukin-1β, Tumor Necrosis Factor-α, prostaglandin-E2, C reactive protein, D-Lactate and intestinal-type fatty acid binding protein 2 [FABP2]), lipopolysaccharide (LPS). matrix metalloproteinase (MMP)-9 levels, S-100B protein levels, quinolinic acid levels, and the ratio between kynurenic and quinolinic acid
Time Frame
3 months
Title
Plasma levels of inflammatory mediators
Description
Interleukin-1β, Tumor Necrosis Factor-α, prostaglandin-E2, C reactive protein, D-Lactate and intestinal-type fatty acid binding protein 2 [FABP2]), lipopolysaccharide (LPS). matrix metalloproteinase (MMP)-9 levels, S-100B protein levels, quinolinic acid levels, and the ratio between kynurenic and quinolinic acid
Time Frame
6 months
Title
Saliva samples
Description
Oral microbial DNA will be used for library preparation and metagenomic shotgun sequencing using the Illumina HiSeq 2500 System. Shotgun metagenomic sequencing can identify bacteria, fungi, and viruses, with a resolution that allows species-level identification. Sequences will be compared to phylogenetic and functional databases to obtain taxonomic and functional profiles.
Time Frame
Baseline
Title
Saliva samples
Description
Oral microbial DNA will be used for library preparation and metagenomic shotgun sequencing using the Illumina HiSeq 2500 System. Shotgun metagenomic sequencing can identify bacteria, fungi, and viruses, with a resolution that allows species-level identification. Sequences will be compared to phylogenetic and functional databases to obtain taxonomic and functional profiles.
Time Frame
3 months
Title
Saliva samples
Description
Oral microbial DNA will be used for library preparation and metagenomic shotgun sequencing using the Illumina HiSeq 2500 System. Shotgun metagenomic sequencing can identify bacteria, fungi, and viruses, with a resolution that allows species-level identification. Sequences will be compared to phylogenetic and functional databases to obtain taxonomic and functional profiles.
Time Frame
6 months
Title
Stool samples
Description
Gut microbial DNA will be used for library preparation and metagenomic shotgun sequencing using the Illumina HiSeq 2500 System. Shotgun metagenomic sequencing can identify bacteria, fungi, and viruses, with a resolution that allows species-level identification. Sequences will be compared to phylogenetic and functional databases to obtain taxonomic and functional profiles.
Time Frame
Baseline
Title
Stool samples
Description
Gut microbial DNA will be used for library preparation and metagenomic shotgun sequencing using the Illumina HiSeq 2500 System. Shotgun metagenomic sequencing can identify bacteria, fungi, and viruses, with a resolution that allows species-level identification. Sequences will be compared to phylogenetic and functional databases to obtain taxonomic and functional profiles.
Time Frame
3 months
Title
Stool samples
Description
Gut microbial DNA will be used for library preparation and metagenomic shotgun sequencing using the Illumina HiSeq 2500 System. Shotgun metagenomic sequencing can identify bacteria, fungi, and viruses, with a resolution that allows species-level identification. Sequences will be compared to phylogenetic and functional databases to obtain taxonomic and functional profiles.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
5.3.1. Inclusion criteria: Age greater or equal to 18 years. Patients with moderate or severe major depression, without severe suicide ideation, as characterized by the Patient Health Questionnaire (PHQ)-9 index (values of 9 or greater) and by the Structured Clinical Interview for DSM-5 - (SCID) will be selected. Subjects with periodontitis stages III or IV, according to the 2018 Classification on periodontal and peri-implant diseases (Papapanou et al., 2018). 5.3.2. Exclusion criteria: Pregnant or breastfeeding women. Diabetes mellitus. Chronic conditions: HIV infection, chronic intake of NSAIDs. Comorbidity with other mental disorders: eating disorders, borderline personality disorders, bipolar disorders, schizophrenia and related disorders, and/or any mental serious disease other than major depression. Severe suicide ideation. Smokers of 10 or more cigarettes per day. Patients who had received periodontal treatment for periodontitis in the last year. Presence of necrotizing periodontal diseases. Presence of less than 3 teeth per quadrant. Antibiotic use in the last 6 months prior to the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elena Figuero, Prof.
Phone
0034913942186
Email
elfiguer@ucm.es
First Name & Middle Initial & Last Name or Official Title & Degree
Juan Carlos Leza Cerro, Prof.
Phone
0034913941478
Email
jcleza@ucm.es
Facility Information:
Facility Name
Faculty of Dentistry, University Complutense of Madrid (UCM)
City
Madrid
ZIP/Postal Code
28034
Country
Spain
Facility Name
Instituto de Psiquiatría y Salud Mental, Hospital Clínico San Carlos
City
Madrid
ZIP/Postal Code
28040
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Impact of Periodontal Therapy on Mental Health Parameters

We'll reach out to this number within 24 hrs