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The Mouth Matters in Mental Health Study

Primary Purpose

Mental Disorders, Severe

Status
Not yet recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Link work intervention
Sponsored by
Lancaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Mental Disorders, Severe focused on measuring Mental Health, Oral Health, Dentistry

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Aged >18 years
  2. Able to provide informed consent
  3. Receipt of care from a Community Mental Health Team (or equivalent service) or Early Intervention Team at the point of referral
  4. No routine and planned dental appointment in the past 3 years. The person should not have accessed a dental service (e.g. high street dentist, special care dentist service) for routine or planned dental care in the past 3 years. This would include any dental examination, diagnosis, advice or treatment (e.g. fillings, root canal, extractions, crowns, dentures, bridges) resulting from a routine (non-emergency) appointment at a dental service. The researchers do not consider emergency dental care (e.g. attendance at A&E, dental hospital) within this definition, although any follow-up routine and planned appointments with a dentist would exclude the person from taking part.

Exclusion criteria:

  1. Inpatient status on a psychiatric or secure ward. The researchers will allow participants in supported living to take part as long as they are in receipt of care from a Community Mental Health Team (or equivalent service) or Early Intervention for Psychosis Service
  2. Immediate risk to self or others operationalised as the presence of active intent or planning to harm oneself or others in the near future (e.g. next month). Where individuals are excluded on this basis, with the person's consent, the researcher will aim to re-contact them and the referrer in approximately 1 month's time (or a time period agreed in collaboration with the individual) to determine if the risk has subsided to a point where they are now eligible.
  3. Enrolled in a dental trial

Sites / Locations

  • Pennine Care NHS Foundation Trust
  • Greater Manchester Mental Health NHS Foundation Trust
  • University of Manchester
  • Lancaster University
  • Lancashire and South Cumbria NHS Foundation Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention group

Treatment as usual group

Arm Description

Participants will receive treatment as usual plus a link work intervention to support access to dental services.

Participants to receive treatment as usual and will not receive the intervention.

Outcomes

Primary Outcome Measures

Recruitment rates - feasibility criteria
Data on ability to recruit randomise 84 participants to target in a 7-month recruitment window. Green ≥80%. Amber 60-79%. Red ≤59%.
Visiting data - feasibility criteria
Percentage of participants with available data on dental visiting via self-report or BSA data. Green ≥80%. Amber 60-79%. Red ≤59%.
Clinical exam - feasibility criteria
Percentage of participants completing the dental examination. Green ≥80%. Amber 60-79%. Red: ≤59%.
Adherence to intervention - feasibility criteria
Percentage of participants receiving intervention ≥1 sessions during nine month window. Green ≥80%. Amber 60-79%. Red ≤59%.
Intervention and trial protocol - feasibility criteria
Qualitative data to understand the acceptability and feasibility of the procedures, assessments, and intervention to inform a full trial and service delivery. This will be via qualitative interviews with service users (participants), research staff (link workers, research assistants), and key stakeholders (referrers, managers, commissioners). Audio recordings of sessions and field notes will also be analysed.
Safety of intervention - feasibility criteria
Monitoring and review of research related serious adverse events (SAEs). The Trial Steering Committee (TSC) will oversee SAEs across treatment arms. The authors will discontinue the trial if the intervention or procedures elevate risk.

Secondary Outcome Measures

Brief Pain Inventory - short form
A questionnaire to assess orofacial pain.
Manchester Orofacial Pain Disability Scale
Pain related disability
Oral Health Impact Profile
Oral health related quality of life
Confidence around dental visiting
Item asking about confidence in visiting the dentist. "How confident are you that you will be able to attend a dental appointment?" (1, no confident; 7, very confident)
Rosenberg Self-esteem Scale (RSES)
Assessing self-esteem
Modified Dental Anxiety Scale
Assessing dental anxiety
Patient Health Questionnaire (PHQ)
Assessing depression
EuroQol 5 Dimension (EQ-5D-5L)
Assessing quality of life
The number of eligible participants able to access free or subsidised dental care
Assessing ability to successfully access free or subsidised dental care collected via the business services authority and self-report.
The number of planned dental appointments attended
The research team will record and report the number of routine dental appointments attended, recorded by both the business services authority and self-report.
Oral health self-management - tooth brushing, mouth wash, and flossing
'How often do you brush your teeth nowadays?' (ordinal five-point scale); 'How long do you brush your teeth for nowadays?' (ordinal five-point scale); 'How often do you clean between your teeth (inter-dental cleaning with floss, inter-dental brushes, tooth picks)?' (ordinal five-point scale); and 'Do you use a fluoride mouth-wash?' (binary)
Self reported attendance at a planned dental appointment
The research team will ask people the following 'Have you attended a dental service since the baseline assessment (nine months ago)? This would include a routine appointment with a dentist or special care dentistry service. It could also include a planned appointment at a dental hospital. However, it would not include an emergency dental appointment.'. Participants will also be asked to provide the dates and times of dental appointments. This outcome will be coded as whether the person has or has not accessed a planned dental appointment via self-report.
Business services authority recorded attendance at a planned dental appointment
NHS England collects information on visiting behaviour via the Business Services Authority. The research team will gain participants consent to extract this data, which the researchers will then match to the participants research data. The business services authority will be used to collect data on whether a planned care appointment has taken place. This data will only pick up National Health Service, and not private, dental appointments. This outcome will be coded as whether the person has or has not accessed a planned dental appointment via the business services authority data.
Number of decayed, missing, or filled teeth (DMFT) via dental examination
An examination for dental caries in permanent teeth will involve examining 32 teeth (i.e. all permanent teeth including wisdom teeth) with a metallic periodontal probe (Community Periodontal Index (CPI) probe) and a plane mouth mirror.
Pulpal involvement, ulceration due to trauma, fistula, and abscess (PUFA) via dental examination
The PUFA score per person is calculated in the same cumulative way as for the DMFT and represents the number of teeth that meet the PUFA diagnostic criteria. Thus, for an adult in our study the score can range from 0 to 32 PUFA.
Modified Plaque Score via dental examination
The locally derived system involves assessing six teeth representative of the entire dentition, for the worst plaque score on each tooth surface from visual examination and, where necessary, the use of a probe to detect the presence of plaque. These six teeth are the UL4 UL1 UR6 LL6 LR1 LR4. Each surface; Interproximal, buccal and lingual or palatal of the six teeth should be viewed in turn and the highest level of visible plaque on each surface should be scored '2'.

Full Information

First Posted
September 8, 2022
Last Updated
September 18, 2022
Sponsor
Lancaster University
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1. Study Identification

Unique Protocol Identification Number
NCT05545228
Brief Title
The Mouth Matters in Mental Health Study
Official Title
A Randomised Feasibility Trial of an Intervention Using Mental Health Support Workers as Link Workers to Improve Dental Visiting in People With Severe Mental Illness: The Mouth in Mind Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2022 (Anticipated)
Primary Completion Date
April 2023 (Anticipated)
Study Completion Date
April 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lancaster University

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
To investigate the feasibility and acceptability of a link work intervention to increase planned dental care visits for patients with severe mental illness, and through this to improve their oral health. To understand what constitutes best practice when delivering link work around dental visiting. To identify what training needs exist for support workers around link work. To determine whether patients with SMI are willing to be randomised to a trial targeting dental visiting. To understand whether it is feasible to collect clinical outcome and planned dental appointment data in this population. To explore if, and how, patients with severe mental illness engage with a link work intervention. To understand the potential factors impacting (e.g. facilitators and barriers) acceptability and delivery.
Detailed Description
Background and study aims Severe mental ill health (SMI) affects around 1% of the population. It includes depression, psychosis, and bipolar disorder. People with experience of SMI are more likely to have problems with their teeth and gums. This includes more missing, filled, and decayed teeth than people without SMI. Having poor oral health can impact a lot of everyday activities like eating, speaking and smiling. It can affect how patients see themselves and their mental health. Dentists can treat many early teeth and gum problems. However, very few people with SMI attend regular dental appointments. Instead, they are more likely to seek help when in crisis and invasive treatments are the only option. Accessing a dentist for people with SMI can be difficult for lots of reasons. People can feel helpless, fearful, or unmotivated to attend. They can have difficulty booking, planning, and getting to appointments. They may struggle to pay for or access free dental care. Unfortunately, existing dental initiatives have not addressed the barriers facing this group. They do not help people with SMI to attend the dentist. The investigators want to help people with SMI to access dental care. The study will use mental health support workers who are already working in the National Health Service (NHS). They will link people receiving care from mental health teams with dental services. The support workers will help people to book, plan, and attend regular dental appointments. They will support patients to apply for financial support. People call this type of support link work. Research has indicated that link work can increase dental visits in people who might not normally attend. Mental health support workers already do link work for other appointments. Link work has been used to help other vulnerable groups of people (e.g. children) around dental care. However, this will be the first use of link work to help people with SMI to attend the dentist. Who can participate? People with a severe mental health difficulties currently accessing secondary care mental health services at the point of referral (e.g. community mental health team, early intervention for psychosis service), but who have not had a routine dental appointment in the past three years. What does the study involve? Participants will be randomly allocated to receiving treatment as usual or treatment as usual plus the link work intervention. This will be decided by chance. The investigators will measure how often people in both groups visit the dentist. They will also assess the state of their teeth and gums. They will collect this data when people come into the study and after nine months. The authors will offer interviews to patients and staff involved in the trial to understand how they found their involvement. What are the possible benefits and risks of participating? The intervention aims to support people to access dental services. However, it is currently untested, which is the reason for doing the research. When is the study starting and how long it is expected to run for? Recruitment for the trial is starting in September 2022 and will run for seven months. The whole project is scheduled to finish in April 2024. Who is funding the study? The National Institute of Health Research (NIHR) Health and Social Care Delivery Research (HS&DR) scheme are funding the project.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mental Disorders, Severe
Keywords
Mental Health, Oral Health, Dentistry

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A feasibility single-blinded randomised controlled trial
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Participants will receive treatment as usual plus a link work intervention to support access to dental services.
Arm Title
Treatment as usual group
Arm Type
No Intervention
Arm Description
Participants to receive treatment as usual and will not receive the intervention.
Intervention Type
Behavioral
Intervention Name(s)
Link work intervention
Intervention Description
Intervention from a link worker to support participants to access dental services.
Primary Outcome Measure Information:
Title
Recruitment rates - feasibility criteria
Description
Data on ability to recruit randomise 84 participants to target in a 7-month recruitment window. Green ≥80%. Amber 60-79%. Red ≤59%.
Time Frame
7 months
Title
Visiting data - feasibility criteria
Description
Percentage of participants with available data on dental visiting via self-report or BSA data. Green ≥80%. Amber 60-79%. Red ≤59%.
Time Frame
9 months
Title
Clinical exam - feasibility criteria
Description
Percentage of participants completing the dental examination. Green ≥80%. Amber 60-79%. Red: ≤59%.
Time Frame
9 months
Title
Adherence to intervention - feasibility criteria
Description
Percentage of participants receiving intervention ≥1 sessions during nine month window. Green ≥80%. Amber 60-79%. Red ≤59%.
Time Frame
9 months
Title
Intervention and trial protocol - feasibility criteria
Description
Qualitative data to understand the acceptability and feasibility of the procedures, assessments, and intervention to inform a full trial and service delivery. This will be via qualitative interviews with service users (participants), research staff (link workers, research assistants), and key stakeholders (referrers, managers, commissioners). Audio recordings of sessions and field notes will also be analysed.
Time Frame
9 months
Title
Safety of intervention - feasibility criteria
Description
Monitoring and review of research related serious adverse events (SAEs). The Trial Steering Committee (TSC) will oversee SAEs across treatment arms. The authors will discontinue the trial if the intervention or procedures elevate risk.
Time Frame
9 Months
Secondary Outcome Measure Information:
Title
Brief Pain Inventory - short form
Description
A questionnaire to assess orofacial pain.
Time Frame
Baseline and 9 month assessments
Title
Manchester Orofacial Pain Disability Scale
Description
Pain related disability
Time Frame
Baseline and 9 month assessments
Title
Oral Health Impact Profile
Description
Oral health related quality of life
Time Frame
Baseline and 9 month assessments
Title
Confidence around dental visiting
Description
Item asking about confidence in visiting the dentist. "How confident are you that you will be able to attend a dental appointment?" (1, no confident; 7, very confident)
Time Frame
Baseline and 9 month assessments
Title
Rosenberg Self-esteem Scale (RSES)
Description
Assessing self-esteem
Time Frame
Baseline and 9 month assessments
Title
Modified Dental Anxiety Scale
Description
Assessing dental anxiety
Time Frame
Baseline and 9 month assessments
Title
Patient Health Questionnaire (PHQ)
Description
Assessing depression
Time Frame
Baseline and 9 month assessments
Title
EuroQol 5 Dimension (EQ-5D-5L)
Description
Assessing quality of life
Time Frame
Baseline and 9 month assessments
Title
The number of eligible participants able to access free or subsidised dental care
Description
Assessing ability to successfully access free or subsidised dental care collected via the business services authority and self-report.
Time Frame
Baseline and 9 month assessments
Title
The number of planned dental appointments attended
Description
The research team will record and report the number of routine dental appointments attended, recorded by both the business services authority and self-report.
Time Frame
Baseline and 9 month assessments
Title
Oral health self-management - tooth brushing, mouth wash, and flossing
Description
'How often do you brush your teeth nowadays?' (ordinal five-point scale); 'How long do you brush your teeth for nowadays?' (ordinal five-point scale); 'How often do you clean between your teeth (inter-dental cleaning with floss, inter-dental brushes, tooth picks)?' (ordinal five-point scale); and 'Do you use a fluoride mouth-wash?' (binary)
Time Frame
Baseline and 9 month assessments
Title
Self reported attendance at a planned dental appointment
Description
The research team will ask people the following 'Have you attended a dental service since the baseline assessment (nine months ago)? This would include a routine appointment with a dentist or special care dentistry service. It could also include a planned appointment at a dental hospital. However, it would not include an emergency dental appointment.'. Participants will also be asked to provide the dates and times of dental appointments. This outcome will be coded as whether the person has or has not accessed a planned dental appointment via self-report.
Time Frame
9 months
Title
Business services authority recorded attendance at a planned dental appointment
Description
NHS England collects information on visiting behaviour via the Business Services Authority. The research team will gain participants consent to extract this data, which the researchers will then match to the participants research data. The business services authority will be used to collect data on whether a planned care appointment has taken place. This data will only pick up National Health Service, and not private, dental appointments. This outcome will be coded as whether the person has or has not accessed a planned dental appointment via the business services authority data.
Time Frame
9 months
Title
Number of decayed, missing, or filled teeth (DMFT) via dental examination
Description
An examination for dental caries in permanent teeth will involve examining 32 teeth (i.e. all permanent teeth including wisdom teeth) with a metallic periodontal probe (Community Periodontal Index (CPI) probe) and a plane mouth mirror.
Time Frame
Baseline and 9 months
Title
Pulpal involvement, ulceration due to trauma, fistula, and abscess (PUFA) via dental examination
Description
The PUFA score per person is calculated in the same cumulative way as for the DMFT and represents the number of teeth that meet the PUFA diagnostic criteria. Thus, for an adult in our study the score can range from 0 to 32 PUFA.
Time Frame
Baseline and 9 months
Title
Modified Plaque Score via dental examination
Description
The locally derived system involves assessing six teeth representative of the entire dentition, for the worst plaque score on each tooth surface from visual examination and, where necessary, the use of a probe to detect the presence of plaque. These six teeth are the UL4 UL1 UR6 LL6 LR1 LR4. Each surface; Interproximal, buccal and lingual or palatal of the six teeth should be viewed in turn and the highest level of visible plaque on each surface should be scored '2'.
Time Frame
Baseline and 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged >18 years Able to provide informed consent Receipt of care from a Community Mental Health Team (or equivalent service) or Early Intervention Team at the point of referral No routine and planned dental appointment in the past 3 years. The person should not have accessed a dental service (e.g. high street dentist, special care dentist service) for routine or planned dental care in the past 3 years. This would include any dental examination, diagnosis, advice or treatment (e.g. fillings, root canal, extractions, crowns, dentures, bridges) resulting from a routine (non-emergency) appointment at a dental service. The researchers do not consider emergency dental care (e.g. attendance at A&E, dental hospital) within this definition, although any follow-up routine and planned appointments with a dentist would exclude the person from taking part. Exclusion criteria: Inpatient status on a psychiatric or secure ward. The researchers will allow participants in supported living to take part as long as they are in receipt of care from a Community Mental Health Team (or equivalent service) or Early Intervention for Psychosis Service Immediate risk to self or others operationalised as the presence of active intent or planning to harm oneself or others in the near future (e.g. next month). Where individuals are excluded on this basis, with the person's consent, the researcher will aim to re-contact them and the referrer in approximately 1 month's time (or a time period agreed in collaboration with the individual) to determine if the risk has subsided to a point where they are now eligible. Enrolled in a dental trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jasper Palmier-Claus, PhD, DClinPsy
Phone
01524 663086
Email
j.palmier-claus@lancaster.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Claire A Hilton, MRes
Phone
01524 593555
Email
c.a.hilton@lancaster.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jasper Palmier-Claus, PhD, DClinPsy
Organizational Affiliation
Lancaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rebecca Harris, BDS, PhD
Organizational Affiliation
University of Liverpool
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pennine Care NHS Foundation Trust
City
Ashton-under-Lyne
State/Province
Great Manchester
ZIP/Postal Code
OL6 7SR
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paul French, PhD
Phone
0161 2472976
Email
p.french@mmu.nhs.uk
Facility Name
Greater Manchester Mental Health NHS Foundation Trust
City
Manchester
State/Province
Great Manchester
ZIP/Postal Code
M25 3BL
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Robert Giffiths, PhD
Phone
0161 7739121
Email
robert.griffiths@gmmh.nhs.uk
Facility Name
University of Manchester
City
Manchester
State/Province
Greater Manchester
ZIP/Postal Code
M13 9PL
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Louise Laverty, Phd
Email
louise.laverty@manchester.ac.uk
Facility Name
Lancaster University
City
Lancaster
State/Province
Lancashire
ZIP/Postal Code
LA1 4YW
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jasper Palmier-Claus, PhD, DClinPsy
Phone
01524 663086
Email
j.palmier-claus@lancaster.ac.uk
First Name & Middle Initial & Last Name & Degree
Claire A Hilton, MRes
Phone
01524 593555
Email
c.a.hilton@lancaster.ac.uk
First Name & Middle Initial & Last Name & Degree
Jasper Palmier-Claus, PhD, DClinPsy
Facility Name
Lancashire and South Cumbria NHS Foundation Trust
City
Preston
State/Province
Lancashire
ZIP/Postal Code
PR2 8DW
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jasper Palmier-Claus, PhD
Phone
01524 663086
Email
j.palmier-claus@lancaster.ac.uk

12. IPD Sharing Statement

Plan to Share IPD
No

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The Mouth Matters in Mental Health Study

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