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An Online Intervention to Address Barriers to IBD Medication Adherence

Primary Purpose

Inflammatory Bowel Disease (IBD)

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
CBT based online intervention to elicit and address perceptual and practical barriers to taking medication.
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Disease (IBD) focused on measuring Inflammatory Bowel Disease (IBD), Crohn's disease, Ulcerative colitis, Cognitive Behavioural Therapy (CBT), Medication adherence

Eligibility Criteria

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

Inclusion Criteria:

  • Age 18 or over.
  • Diagnosis of IBD (Crohn's Disease or Ulcerative Colitis or Indeterminate Colitis).
  • Currently prescribed one or more of the following medications for IBD: azathioprine, mesalazine, and adalimumab.

Exclusion Criteria:

  • We will exclude people who are for any reason unable to make an informed decision about taking part and people who do not wish to complete follow-up questionnaires.
  • People who declare that they do not understand written English. This is a pilot feasibility study that aims to assess the effectiveness and acceptability of an online CBT based intervention in English.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    CBT based online intervention

    Control group

    Arm Description

    CBT based online intervention to elicit and address perceptual and practical barriers to taking medication.

    Care as Usual. Participants in the control group will be able to access the online intervention after they complete their last follow-up questionnaire.

    Outcomes

    Primary Outcome Measures

    Change in Beliefs about Medicines Questionnaire (BMQ)
    The BMQ (Horne and Weinman, 1999) has been validated for use with people with chronic conditions. It comprises a scale that measures beliefs about medication prescribed specifically for IBD and a general scale that evaluates beliefs that medicines are harmful, addictive, poisons.

    Secondary Outcome Measures

    Change in Medication Adherence Report Scale (MARS)
    The MARS scale (Horne and Hankins 1997) is extensively used as a measure of adherent behaviours in a variant of illness populations. The MARS attempts to diminish the social pressure on patients to under-report non-adherence by phrasing adherence questions in a non-threatening manner and assuring them that responses are anonymous and confidential.
    Change in Hospital Anxiety and Depression questionnaire (HADS)
    The HADS scale (Zigmond and Snaith 1983) is a reliable and valid instrument for detecting states of depression and anxiety.
    Change in Visual Analogue measure of adherence
    Self-reported estimation of the % of medication taken over the last 4 weeks.
    Change in Brief Illness Perception Questionnaire (IPQ)
    The brief IPQ (Broadbent, Petrie et al. 2006) has demonstrated adequate test-retest reliability and validity.
    Change in Satisfaction with Information about Medicines Scale (SIMS)
    The SIMS scale (Horne, Hankins et al. 2001) is a valid and reliable instrument for assessing how well the needs for medicines information in patient are being covered.
    Change in Marlow-Crowne Social Desirability Scale-Form C (M-C Form C) (Reynolds 1982)
    The Marlow-Crowne Social Desirability Scale-Form C (Reynolds 1982) is a measure of social desirability as a response tendency and it has been proved reliable and consistent (Nordholm 1974; Crino, Rubenfeld et al. 1985; Barger 2002).
    Change in Short Inflammatory Bowel Disease Questionnaire
    The SIBDQ is a valid and reliable tool able to detect meaningful clinical changes in the health related quality of life of individuals with both Crohn's disease and Ulcerative colitis. It measures physical, social, and emotional status (the scores go from 10 to 70, poor to good quality of life).

    Full Information

    First Posted
    October 11, 2012
    Last Updated
    May 10, 2013
    Sponsor
    University College, London
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01852097
    Brief Title
    An Online Intervention to Address Barriers to IBD Medication Adherence
    Official Title
    A Pilot Randomised Controlled Trial to Determine the Feasibility, Acceptability and Effectiveness of a CBT Based Online Intervention to Address Practical and Perceptual Barriers to Medication Adherence in Inflammatory Bowel Disease.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2013
    Overall Recruitment Status
    Unknown status
    Study Start Date
    May 2013 (undefined)
    Primary Completion Date
    November 2013 (Anticipated)
    Study Completion Date
    January 2014 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University College, London

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Background Inflammatory Bowel Disease (IBD) is a group of lifelong and relapsing inflammatory conditions that usually affect the colon and the small intestine. Between 30 to 45% of patients with IBD do not take their treatment as prescribed by their health care team (Jackson, Clatworthy et al. 2010). The Perceptions and Practicalities Approach (PAPA) provides a theoretical framework to develop adherence interventions that are patient-centred (Horne, 2001). Unintentional non-adherence occurs when the patient wants to take the medication but there are barriers beyond their control, such as not understanding the instructions (practical barriers). Intentional non-adherence is the result of the beliefs affecting the patient's motivation to continue with treatment (perceptual barriers). Aims To develop an internet-based intervention to address perceptual and practical barriers to adherence to medicine for IBD. To determine whether the intervention is effective based on change in both types of barriers. Plan of Investigation The inclusion criteria are: age 18 or over; diagnosis of IBD; currently prescribed azathioprine, mesalazine, and/or adalimumab. 240 participants identified via Crohn's and Colitis UK and through two NHS IBD clinics will take part in the study. An online pilot Randomised Controlled Trial will allocate the participants either to a Cognitive Behavioural Therapy (CBT) based online intervention or Treatment as Usual group. On first visiting the website, participants will be screened for eligibility and asked for consent before answering the questionnaires. The website will assign intervention modules to be completed based on an individual's profile. Outcomes: Beliefs about Medicines scores will be measured at baseline, 1 month and 3 month follow-ups. Potential Impact A CBT based online intervention tailored to personal needs and concerns may benefit a large number of patients with low costs for the national healthcare services. A website can be accessed at a time and place convenient to the patient.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Inflammatory Bowel Disease (IBD)
    Keywords
    Inflammatory Bowel Disease (IBD), Crohn's disease, Ulcerative colitis, Cognitive Behavioural Therapy (CBT), Medication adherence

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Investigator
    Allocation
    Randomized
    Enrollment
    240 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    CBT based online intervention
    Arm Type
    Experimental
    Arm Description
    CBT based online intervention to elicit and address perceptual and practical barriers to taking medication.
    Arm Title
    Control group
    Arm Type
    No Intervention
    Arm Description
    Care as Usual. Participants in the control group will be able to access the online intervention after they complete their last follow-up questionnaire.
    Intervention Type
    Behavioral
    Intervention Name(s)
    CBT based online intervention to elicit and address perceptual and practical barriers to taking medication.
    Intervention Description
    The general approach to the intervention is the following: Assess and profile individual perceptual and practical barriers to medication for IBD using validated questionnaires. Give feedback to individuals on their questionnaire responses. Provide individualised advice to address doubts, misconceptions and concerns for currently prescribed medications. Provide advice on overcoming practical barriers. Send motivational messages (and reminders if applicable) by email or text based on the unique profile of each participant. Provide information about how to raise concerns with medical practitioners and how to get the most from a medical consultation.
    Primary Outcome Measure Information:
    Title
    Change in Beliefs about Medicines Questionnaire (BMQ)
    Description
    The BMQ (Horne and Weinman, 1999) has been validated for use with people with chronic conditions. It comprises a scale that measures beliefs about medication prescribed specifically for IBD and a general scale that evaluates beliefs that medicines are harmful, addictive, poisons.
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up
    Secondary Outcome Measure Information:
    Title
    Change in Medication Adherence Report Scale (MARS)
    Description
    The MARS scale (Horne and Hankins 1997) is extensively used as a measure of adherent behaviours in a variant of illness populations. The MARS attempts to diminish the social pressure on patients to under-report non-adherence by phrasing adherence questions in a non-threatening manner and assuring them that responses are anonymous and confidential.
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up
    Title
    Change in Hospital Anxiety and Depression questionnaire (HADS)
    Description
    The HADS scale (Zigmond and Snaith 1983) is a reliable and valid instrument for detecting states of depression and anxiety.
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up
    Title
    Change in Visual Analogue measure of adherence
    Description
    Self-reported estimation of the % of medication taken over the last 4 weeks.
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up.
    Title
    Change in Brief Illness Perception Questionnaire (IPQ)
    Description
    The brief IPQ (Broadbent, Petrie et al. 2006) has demonstrated adequate test-retest reliability and validity.
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up.
    Title
    Change in Satisfaction with Information about Medicines Scale (SIMS)
    Description
    The SIMS scale (Horne, Hankins et al. 2001) is a valid and reliable instrument for assessing how well the needs for medicines information in patient are being covered.
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up
    Title
    Change in Marlow-Crowne Social Desirability Scale-Form C (M-C Form C) (Reynolds 1982)
    Description
    The Marlow-Crowne Social Desirability Scale-Form C (Reynolds 1982) is a measure of social desirability as a response tendency and it has been proved reliable and consistent (Nordholm 1974; Crino, Rubenfeld et al. 1985; Barger 2002).
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up
    Title
    Change in Short Inflammatory Bowel Disease Questionnaire
    Description
    The SIBDQ is a valid and reliable tool able to detect meaningful clinical changes in the health related quality of life of individuals with both Crohn's disease and Ulcerative colitis. It measures physical, social, and emotional status (the scores go from 10 to 70, poor to good quality of life).
    Time Frame
    Baseline, 1 month follow-up, 3 month follow-up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 18 or over. Diagnosis of IBD (Crohn's Disease or Ulcerative Colitis or Indeterminate Colitis). Currently prescribed one or more of the following medications for IBD: azathioprine, mesalazine, and adalimumab. Exclusion Criteria: We will exclude people who are for any reason unable to make an informed decision about taking part and people who do not wish to complete follow-up questionnaires. People who declare that they do not understand written English. This is a pilot feasibility study that aims to assess the effectiveness and acceptability of an online CBT based intervention in English.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Alice Sibelli, MSc. Health Psychology
    Phone
    +44(0)20 7874 1282
    Email
    a.sibelli@ucl.ac.uk
    First Name & Middle Initial & Last Name or Official Title & Degree
    Rob Horne, Prof. of Behavioural Medicine
    Phone
    +44 (0)20 7874 1281
    Email
    r.horne@ucl.ac.uk

    12. IPD Sharing Statement

    Links:
    URL
    http://www.ucl.ac.uk/jro
    Description
    Sponsor
    URL
    http://www.ucl.ac.uk/pharmacy
    Description
    UCL School of Pharmacy official website

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    An Online Intervention to Address Barriers to IBD Medication Adherence

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