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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06116331
Other study ID # 33844
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2023
Est. completion date December 31, 2024

Study information

Verified date October 2023
Source King's College London
Contact Natasha Seaton, MSc
Phone 0207 188 1189
Email natasha.seaton@kcl.ac.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 170
Est. completion date December 31, 2024
Est. primary completion date December 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

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

Locations

Country Name City State
United Kingdom King's College London London

Sponsors (2)

Lead Sponsor Collaborator
King's College London Medical Research Council

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Psychological distress: Patient Health Questionnaire Anxiety and Depression Scale (PHQ-ADS) 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. Month 0, Month 6, Month 12
Primary Depression: Patient Health Questionnaire - (PHQ-9) Depression. Min score = 0, Max score = 27, with higher scores indicating greater depression. Month 0, Month 6, Month 12
Primary Anxiety: Generalised Anxiety Disorder scale (GAD-7) Anxiety. Min score = 0, Max score = 21, with higher scores indicating greater anxiety Month 0, Month 6, Month 12
Primary Fecal Calprotectin Measure of intestinal inflammation, higher levels indicate greater inflammation. Month 0, Month 6
Primary Health service use 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. Month 0, Month 6, Month 12
Primary IBD activity 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.
Month 0, Month 6, Month 12
Secondary Body Mass Index Weight (in kg) and Height (in m) will be combined to calculate BMI (weight in kg / (height in m)^2 Month 0, Month 6, Month 12
Secondary Smoking status Current smoking status, including amount of cigarettes consumed per day. Month 0, Month 6, Month 12
Secondary Alcohol Consumption Number of units drunk in the past week. Month 0, Month 6, Month 12
Secondary Physical activity: International Physical Activity Questionnaire 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. Month 0, Month 6, Month 12
Secondary IBD medication Current medication and dose. Month 0, Month 6, Month 12
Secondary IBD flares Frequency and severity (4-point scale) of IBD flares (in last 6 months) Month 0, Month 6, Month 12
Secondary Sleep - the Pittsburgh Sleep Quality Index (PSQI) Sleep quality in the last month. Min=0, max=21, with higher scores indicating worse sleep quality. Month 0, Month 6, Month 12
Secondary Diet - Healthy Eating Assessment 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. Month 0, Month 6, Month 12
Secondary IBD quality of life - short Inflammatory Bowel Disease Questionnaire (sIBDQ) 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. Month 0, Month 6, Month 12
Secondary Medication Adherence - Medication Adherence Report Scale (MARS) 5-item scale on a 5-point scale.Mix=0, Max=20, with higher scores indicating better adherence. Month 0, Month 6, Month 12
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