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Completed

NCT Number: NCT03162575

Mindfulness-Based Cognitive Therapy for Fatigue in Inflammatory Bowel Disease Patients: a Randomized Controlled Trial

The current study aims to investigate the efficacy of Mindfulness-Based Cognitive Therapy (MBCT) for reducing fatigue in Inflammatory Bowel Disease patients in remission.

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Key information

Conditions

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UMCG

Groningen, Netherlands

About this study

Fatigue is highly prevalent in patients with inflammatory bowel disease (IBD, i.e. Crohn's disease and ulcerative colitis), and may negatively impact patients' illness management, treatment adherence, and quality of life. Given this burden, effective treatment for reducing fatigue in IBD patients is warranted. A promising psychological treatment is Mindfulness-Based Cognitive Therapy (MBCT). MBCT is a standardized, highly structured eight-week group program for reducing stress, depression, fatigue and/or pain. Several meta-analyses have demonstrated the effectiveness of MBCT in reducing psychological complaints and improving quality of life. Moreover, in patients with cancer or chronic fatigue syndrome, there is preliminary evidence that MBCT can be effective in reducing fatigue. Given this lack of evidence for the efficacy of MBCT in reducing fatigue in general and the specific and strongly illness-related nature of fatigue in patients with IBD and characteristics of the illness, including its lifelong and relapsing nature, there is a need to verify whether MBCT is effective in reducing fatigue in IBD patients with severe fatigue.

This randomized controlled trial (RCT) aims to investigate the efficacy of Mindfulness-Based Cognitive Therapy (MBCT) in reducing fatigue in severely fatigued IBD patients. Additionally, the effects of MBCT on clinically relevant secondary outcomes will be examined: fatigue interference, mood, IBD-specific quality of life, sleep quality, labor participation. Also patients' satisfaction will be assessed. Moreover, mediators and moderators will be examined to increase the understanding of why and for whom MBCT is particularly effective.

A randomized controlled trial will be performed, including two conditions: MBCT and a waitlist control group (who will receive MBCT after a waiting period of three months). The study sample will consist of 128 adult patients with IBD in remission and experiencing severe fatigue.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosed with either Crohn's disease or Ulcerative Colitis
  • Currently in remission
  • No expectation of a surgery in the upcoming three months
  • Score on the subscale 'subjective fatigue' of the CIS (8 items) ≥ 35 (i.e. indicating severe fatigue)
  • Age ≥ 18 and ≤ 75 years at the time of study entrance
  • Being able to attend eight weekly group sessions of 2.5 hours in the hospital
  • Being able to read, write, and speak Dutch.
  • Written informed consent

Exclusion criteria

  • Severe cognitive, neurological or psychiatric co-morbidity that could interfere with patients' participation and/or warrant other treatment, including acute suicidal ideations or behavior, diagnosis of schizophrenia or history of psychotic complaints, bipolar disorder, severe personality disorder, or history of clinically significant drug abuse or substance dependence
  • Pregnancy
  • Anemia (i.e. Hb < 7.4 for women, < 8.1 for men)
  • Change in IBD medication (i.e. use of steroids) within 1 month before study entry
  • Currently receiving psychological treatment for fatigue or for psychological/psychiatric problems.

Treatment and study plan

Mindfulness-Based Cognitive Therapy

Behavioral

Structured MBCT intervention based on the protocol of Williams, Teasdale, and Segal (2002)

Other names: MBCT

Primary outcomes

  1. Change in fatigue

    Time frame: Change from baseline in severity of fatigue symptoms at 3 months, 6 months and 12 months

    Fatigue will be assessed with the Checklist Individual Strength (CIS-20)

Secondary outcomes

  1. Change in fatigue interference

    Time frame: Change from baseline in fatigue interference at 3 months, 6 months, and 12 months

    Fatigue interference will be measured by the Fatigue Symptom Inventory (FSI)

  2. Change in anxiety

    Time frame: Change from baseline in generalized anxiety at 3 months, 6 months, and 12 months

    Anxiety will be measured by Generalised Anxiety Disorder Assessment (GAD 7)

  3. Change in depression

    Time frame: Change from baseline in depression at 3 months, 6 months, and 12 months

    Depression will be measured by Beck Depression Inventory-II (BDI-II)

  4. Change in IBD-specific quality of life

    Time frame: Change from baseline in quality of life at 3 months, 6 months, and 12 months

    IBD-specific quality of life will be measured by the IBD-Q

  5. Change in sleep quality

    Time frame: Change from baseline in sleep quality at 3 months, 6 months, and 12 months

    Sleep quality will be measured by the Pittsburgh Sleep Quality Index

  6. Change in labor participation

    Time frame: Change from baseline in labor participation at 3 months, 6 months, and 12 months

    Labor participation will be assessed with several questions

  7. Satisfaction with treatment

    Time frame: Assessed at 3 months

    Satisfaction with treatment will be assessed with several questions

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Registry information

Official study title

The Possible Beneficial Effects of Mindfulness-Based Cognitive Therapy (MBCT) in Fatigued Adult Patients With Inflammatory Bowel Disease (IBD)

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
May 22, 2017
Registry last updated
Aug 5, 2024

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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