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Completed

NCT Number: NCT00934973

Management of Irritable Bowel Syndrome in Primary Care (MIBS Trial)

Aims:

1. To pilot an randomized, controlled trial (RCT) to assess the effectiveness of the commonly prescribed medications in UK general practice for IBS: mebeverine (anti-spasmodic) and methylcellulose (bulking-agent) and of the patient CBT based self-management website. 2. To assess the level of support needed for patients using the patient CBT based self-management website for IBS (i.e., initial 30 minute telephone support session with a nurse and email support or not).

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Key information

Age range

16 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Southampton

Southampton, Hampshire, SO17 1JB, United Kingdom

About this study

Background:

Irritable bowel syndrome (IBS) affects 10-22% of the United Kingdom (UK) population, with National Health Service (NHS) costs over £200 million a year. Abdominal pain, bloating and altered bowel habit affect quality of life, social functioning and time off work. Current general practitioner (GP) treatment relies on a positive diagnosis, reassurance, lifestyle advice and drug therapies, but many suffer ongoing symptoms.

A recent Cochrane review highlighted the lack of research evidence for IBS drugs. Neither GPs, nor patients have good evidence to inform prescribing decisions. However, IBS drugs are widely used: NHS costs 2005 of nearly £10 million for mebeverine and over £8 million for fiber-based bulking agents.

Cognitive behavioral therapy (CBT) and self-management can be helpful, but poor availability in the NHS restricts its use. Development of web-based CBT could increase access without increased costs.

Plan of Investigation:

135 patients aged 16-60 years with IBS symptoms fulfilling the Rome III criteria, recruited via GP practices, will be randomised to: mebeverine, methylcellulose or placebo for 6 weeks and to the CBT based website with a nurse telephone session and email support, website with minimal support, or no website, thus creating 9 groups.

Outcomes: Irritable bowel symptom severity scale and IBS-QOL will be measured at baseline, 6 and 12 weeks. An intention to treat analysis will be undertaken by analysis of covariance (ANCOVA) for a factorial trial.

Potential Impact:

Development of a web-based self-management CBT program for IBS developed in partnership with patients has the potential to benefit large numbers of patients with low cost to the NHS. CBT has been shown to be of benefit for IBS but it's availability is limited due to the high cost and therapist time required for face-to-face CBT. A website can be accessed at a time and place convenient to the patient and the CBT program undertaken at a pace determined by patient needs. The website could be used as a long term support for self-management.

Determining the effectiveness of commonly used drug treatments will help patients and doctors in making informed treatment decisions regarding the drug management of IBS symptoms, enabling better targeting of treatment to those who may benefit.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 16 to 60 years with symptoms of irritable bowel syndrome that fulfill the Rome III criteria

Exclusion criteria

  • Atypical symptoms (unexplained weight loss, rectal bleeding)
  • Diagnosis of inflammatory bowel disease, coeliac disease or peptic ulcer disease
  • Pregnant or breast feeding
  • Currently taking or allergy to mebeverine or methylcellulose

Treatment and study plan

Mebeverine

Drug

overencapsulated mebeverine 135 mg tds for 6 weeks

methylcellulose

Drug

overencapsulated methylcellulose 3 tablets bd for 6 weeks

Placebo

Drug

overencapsulated placebo tablets 1 tds for 6 weeks

CBT website with support

Behavioral

cognitive behavioral therapy with nurse telephone session and email support

No website

Behavioral

No CBT website

CBT website with minimal support

Behavioral

Primary outcomes

  1. IBS Symptom Severity Score

    Time frame: Baseline, 6 and 12 weeks

  2. IBS QOL

    Time frame: Baseline, 6 and 12 weeks

    Quality of life

Secondary outcomes

  1. Subjects Global Assessment of relief

    Time frame: 6 weeks and 12 weeks

    Subjects global assessment of relief

  2. Enablement

    Time frame: 6 and 12 weeks

    Assessment of Enablement

  3. HADs

    Time frame: Baseline, 6 and 12 weeks

    Hospital Anxiety and Depression Score

Sponsors and collaborators

Lead sponsor

Hazel Everitt

Other

Collaborators

  • National Institute for Health Research, United Kingdom

Registry information

Official study title

Management of Irritable Bowel Syndrome in Primary Care: Feasibility Randomised Controlled Trial of Mebeverine, Methylcellulose, Placebo and a Patient Self-management Cognitive Behavioural Therapy Website. (MIBS Trial)

Acronym: MIBS

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Jul 8, 2009
Registry last updated
Apr 30, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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