The Mind-Body IBD Study: Understanding the Mind-body Connection in IBD

Sponsor
King's College London (Other)
Overall Status
Recruiting
CT.gov ID
NCT06116331
Collaborator
Medical Research Council (Other)
170
1
21
8.1

Study Details

Study Description

Brief Summary

An aspect of IBD care that is often overlooked is mental health treatment. Common mental health problems, such as anxiety and depression are very common in IBD, with a meta-analysis estimating prevalence as high as 25.2% for depression and 32.1% for anxiety. The prevalence of anxiety and depression increases when individuals with active disease are considered, with rates as high as 57.6% for anxiety and 38.9% for depression. Comorbid depression and anxiety in IBD is associated with greater symptom severity, even when statistically controlling for disease activity; more frequent and expensive emergency department visits and inpatient stays, higher costs relating to IBD-related surgery, medication and personal expenditure; noncompliance with medical treatment and finally, increased likelihood of experiencing flares.

However, very few studies attempt to unpick the precise mechanism of these bidirectional relationships.

Indeed, depression and anxiety may have direct effects on physical health through inflammatory or psychoneuroimmunological pathways. Very few studies investigate the longitudinal brain-gut relationship with regards to objective measures of inflammation. Additionally, the indirect effects of mental health are often overlooked. Depression and anxiety are routinely associated with health behaviours, such as diet, physical activity, sleep, and tobacco/alcohol use.These health behaviours are important factors, given their impact on physical health outcomes. Therefore, a thorough investigation is required to ascertain the precise mechanisms that underpin the bidirectional relationship between depression/anxiety and inflammation/physical health, as this will enable practitioners and researchers to establish non-invasive, behavioural treatment targets for this patient group.

AIM The broad aim of this project is to explore whether anxiety/depression has a direct or indirect (via health behaviours) on i) inflammation levels ii) clinical activity and iii) healthcare usage at follow-up, in a population of IBD patients. A secondary aim of the project will be to explore whether changes in disease activity, as measured by self-report measures and faecal calprotectin, explains changes in anxiety and depression symptoms at follow up.

Condition or Disease Intervention/Treatment Phase
  • Other: Data collection

Detailed Description

Participants will be asked to answer online questionnaires at 3 time points, 6 months apart. They will also be asked to do an at-home stool sample test at the first two time points.

Study Design

Study Type:
Observational
Anticipated Enrollment :
170 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Mind-Body IBD Study: Understanding the Bidirectional Relationship Between Depression and Anxiety With Physical Health Outcomes and Inflammation
Actual Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Participants

Participants will complete 3 online questionnaires at 6 month intervals. At the first two time points they will also be asked to submit 2 at home stool sample tests, to assess fecal calprotectin.

Other: Data collection
Participants will answer questionnaires and submit stool samples.

Outcome Measures

Primary Outcome Measures

  1. Psychological distress: Patient Health Questionnaire Anxiety and Depression Scale (PHQ-ADS) [Month 0, Month 6, Month 12]

    The PHQ-ADS is a composite measure of the Generalised Anxiety Disorder questionnaire (GAD-7) and the Patient Health Questionnaire (PHQ-9). Min score = 0, Max score = 48, with higher scores indicating higher levels of distress.

  2. Depression: Patient Health Questionnaire - (PHQ-9) [Month 0, Month 6, Month 12]

    Depression. Min score = 0, Max score = 27, with higher scores indicating greater depression.

  3. Anxiety: Generalised Anxiety Disorder scale (GAD-7) [Month 0, Month 6, Month 12]

    Anxiety. Min score = 0, Max score = 21, with higher scores indicating greater anxiety

  4. Fecal Calprotectin [Month 0, Month 6]

    Measure of intestinal inflammation, higher levels indicate greater inflammation.

  5. Health service use [Month 0, Month 6, Month 12]

    4 service use items (GP, psychologist, emergency care, secondary care service) from the client service receipt inventory (CSRI) will be used. Frequency and duration of particular services will be recorded, from which a total time will be calculated. There is no maximum value. Higher scores indicate more health service time used.

  6. IBD activity [Month 0, Month 6, Month 12]

    For Crohn's Disease patients: The Patient-Reported Outcomes for the Assessment of Crohn's Disease Activity (PRO-CD). The scale contains two sub-scales: 1) bowel signs and symptoms, 2) functional symptoms. Each scale is scored separately. There is no total score for the PRO-CD. The first sub-scale starts at 0 and has no maximum value, with greater scores indicating greater bowel signs/symptoms. The second subscale ranges from 0-21, with higher scores indicating greater functional symptoms. For Ulcerative Colitis / unclassified patients: The Patient-Reported Outcomes for Assessment of Ulcerative Colitis (PRO-UC). The scale has 9-items and includes two scales: 1) Bowel signs/symptoms and 2) functional symptoms. The first sub-scale starts at 0 and has no maximum value, with greater scores indicating greater bowel signs/symptoms. The second subscale ranges from 0-21, with higher scores indicating greater functional symptoms.

Secondary Outcome Measures

  1. Body Mass Index [Month 0, Month 6, Month 12]

    Weight (in kg) and Height (in m) will be combined to calculate BMI (weight in kg / (height in m)^2

  2. Smoking status [Month 0, Month 6, Month 12]

    Current smoking status, including amount of cigarettes consumed per day.

  3. Alcohol Consumption [Month 0, Month 6, Month 12]

    Number of units drunk in the past week.

  4. Physical activity: International Physical Activity Questionnaire [Month 0, Month 6, Month 12]

    Physical activity. There are three subscales (vigorous activity, moderate activity and lower-level activity). Scores will be in minutes. Higher scores will indicate more physical activity performed.

  5. IBD medication [Month 0, Month 6, Month 12]

    Current medication and dose.

  6. IBD flares [Month 0, Month 6, Month 12]

    Frequency and severity (4-point scale) of IBD flares (in last 6 months)

  7. Sleep - the Pittsburgh Sleep Quality Index (PSQI) [Month 0, Month 6, Month 12]

    Sleep quality in the last month. Min=0, max=21, with higher scores indicating worse sleep quality.

  8. Diet - Healthy Eating Assessment [Month 0, Month 6, Month 12]

    8-item simplified food frequency questionnaire designed for use in primary care settings. The tool will be adapted so that each item is score 1-5. Mix=8, max=40, with higher scores indicating better diet quality.

  9. IBD quality of life - short Inflammatory Bowel Disease Questionnaire (sIBDQ) [Month 0, Month 6, Month 12]

    The sIBDQ is a ten-item questionnaire that covers four domains: bowel symptoms, systemic symptoms, emotional health, and social functions. Min=10, max=70, with a lower score indicating lower quality of life.

  10. Medication Adherence - Medication Adherence Report Scale (MARS) [Month 0, Month 6, Month 12]

    5-item scale on a 5-point scale.Mix=0, Max=20, with higher scores indicating better adherence.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Self-reported diagnosis of IBD (pseudo-confirmed with participant's self-reported IBD medication or medication history)

  2. Willing and able to give informed consent and participate in the study

  3. Aged 18 and over

  4. Sufficient command of written and spoken English to understand study procedures and documents, and complete self-report questionnaires

  5. UK resident (GP registered)

  6. Email address, telephone number and postal address to enable all study procedures

  7. Experience at least one flare (requiring medical escalation or medication change) within the last two years

Exclusion Criteria:
  1. Under 18 years

  2. Lives outside of the UK

  3. Insufficient command of English to understand study documents and procedures

  4. Not able to give informed consent Regular use of non-steroidal anti-inflammatory drugs (NSAIDs) in the last two weeks.

  5. People with a cancer diagnosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 King's College London London United Kingdom SE1 9RT

Sponsors and Collaborators

  • King's College London
  • Medical Research Council

Investigators

  • Principal Investigator: Rona Moss-Morris, PhD, King's College London

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
King's College London
ClinicalTrials.gov Identifier:
NCT06116331
Other Study ID Numbers:
  • 33844
First Posted:
Nov 3, 2023
Last Update Posted:
Nov 3, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by King's College London
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 3, 2023