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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01852097
Other study ID # 12/0210
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 11, 2012
Last updated May 10, 2013
Start date May 2013
Est. completion date January 2014

Study information

Verified date February 2013
Source University College, London
Contact Alice Sibelli, MSc. Health Psychology
Phone +44(0)20 7874 1282
Email a.sibelli@ucl.ac.uk
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Interventional

Clinical Trial 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

1. To develop an internet-based intervention to address perceptual and practical barriers to adherence to medicine for IBD.

2. 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 240
Est. completion date January 2014
Est. primary completion date November 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Intervention

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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University College, London

Outcome

Type Measure Description Time frame Safety issue
Primary 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. Baseline, 1 month follow-up, 3 month follow-up No
Secondary 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. Baseline, 1 month follow-up, 3 month follow-up No
Secondary 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. Baseline, 1 month follow-up, 3 month follow-up No
Secondary Change in Visual Analogue measure of adherence Self-reported estimation of the % of medication taken over the last 4 weeks. Baseline, 1 month follow-up, 3 month follow-up. No
Secondary Change in Brief Illness Perception Questionnaire (IPQ) The brief IPQ (Broadbent, Petrie et al. 2006) has demonstrated adequate test-retest reliability and validity. Baseline, 1 month follow-up, 3 month follow-up. No
Secondary 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. Baseline, 1 month follow-up, 3 month follow-up No
Secondary 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). Baseline, 1 month follow-up, 3 month follow-up No
Secondary 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). Baseline, 1 month follow-up, 3 month follow-up No
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