MBMCrohn: Effect of a Stress Reduction and Lifestyle Modification Programme on the Quality of Life of Crohn's Disease Patients

Sponsor
Jost Langhorst (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05182645
Collaborator
Sozialstiftung Bamberg (Other), University of Wuerzburg (Other), Wuerzburg University Hospital (Other), Bavarian State Ministry of Health and Care (Other)
42
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2
21
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Study Details

Study Description

Brief Summary

Patients with crohn's disease often suffer significant limitations to their quality of life, which are also conditioned by particular stress and psychosocial accompanying symptoms of the disease. A multimodal program for stress-reduction and lifestyle-modification has been shown to be effective in promoting the quality of life in patients with uncreative colitis. The study will examine the promotion of the quality of life of patients with crohn's disease and the positive Influence on stress, psychological symptoms and physiological parameters.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: lifestyle-modification
  • Behavioral: waiting control group
N/A

Detailed Description

40 patients with ulcerative colitis will be randomized in an Intervention group and a control group for 10 weeks. The primary outcome is the feasibility of the study, the intervention and the examinations. The Secondary outcomes are disease-specific quality of life, disease-activity, stress, psychological symptoms, inflammatory parameters, disease activity parameters, bowel parameter and the microbiome. As qualitative parameters, the influence of the disease on everyday life and the experience/ impact/ implementability of the programme will be investigated. Lastly, undesirable events will be recorded.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Waiting Control Group DesignWaiting Control Group Design
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
MBMCrohn: Die Wirkung Eines Stressreduktion- Und Lebensstilmodifikations-programms Auf Die Lebensqualität Von Patienten Mit Morbus Crohn- Eine Machbarkeitsstudie
Actual Study Start Date :
Jul 1, 2020
Anticipated Primary Completion Date :
Mar 31, 2022
Anticipated Study Completion Date :
Mar 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: lifestyle-modification

Once a week for 10 weeks with a circumference of 60 hours with mindfulness-based stress reduction and further process of the Mind / body medicine.

Behavioral: lifestyle-modification
The group intervention is carried out once a week for 10 weeks for a total of 60 hours with elements of mindfulness-based stress reduction (MBSR) and further process of the mind / body medicine. In this project, this program will be adapted to the specific needs of crohn's disease patients.

Active Comparator: waiting control group

A unique education unit within the scope of 3 hours on the influence of lifestyle factors on the disease and self-help materials for the independent training. After the follow-up measurement opportunity to participate in the program.

Behavioral: waiting control group
Participants in this group receive a one-time education unit within the scope of 3 hours on the influence of lifestyle factors on the disease, also self-help materials for independent training offered. Following the follow-up measure also this group is given the opportunity to participate in the multimodal stress reduction- and lifestyle modification program.

Outcome Measures

Primary Outcome Measures

  1. Recruitment success [week 48]

    Proportion of people responding to appeals for studies

  2. Willingness to participate [week 48]

    Proportion of people which actually agreed in relation to the proportion of people which responded to the appeal.

  3. Attendance [week 48]

    Proportion of people which actually attend the study

  4. Loss of participants over the study period [week 48]

    Proportion of people who quit during the study

Secondary Outcome Measures

  1. Disease-specific quality of life by IBD-Q [week 0]

    Inflammatory Bowel Disease Questionnaire (IBD-Q), Recording on 7-point Likert scale, high values mean good, low values a reduced quality of life (1=worst score, 7=best score)

  2. Disease-specific quality of life by IBD-Q [week 12]

    Inflammatory Bowel Disease Questionnaire (IBD-Q), Recording on 7-point Likert scale, high values mean good, low values a reduced quality of life (1=worst score, 7=best score)

  3. Disease-specific quality of life by IBD-Q [week 36]

    Inflammatory Bowel Disease Questionnaire (IBD-Q), Recording on 7-point Likert scale, high values mean good, low values a reduced quality of life (1=worst score, 7=best score)

  4. Disease-specific quality of life by IBD-Q [week 48]

    Inflammatory Bowel Disease Questionnaire (IBD-Q), Recording on 7-point Likert scale, high values mean good, low values a reduced quality of life (1=worst score, 7=best score)

  5. Generic quality of life by SF-36 [week 0]

    Short Form Health 36 (SF-36) shows health-related quality of life, 36 items in 8 categories, 25% of the items must be filled in per category for evaluation. Lower sum score correlates with lower quality of life; higher sum score correlates with better quality of life.

  6. Generic quality of life by SF 36 [week 12]

    Short Form Health 36 (SF-36) shows health-related quality of life, 36 items in 8 categories, 25% of the items must be filled in per category for evaluation. Lower sum score correlates with lower quality of life; higher sum score correlates with better quality of life.

  7. Generic quality of life by SF36 [week 36]

    Short Form Health 36 (SF-36) shows health-related quality of life, 36 items in 8 categories, 25% of the items must be filled in per category for evaluation. Lower sum score correlates with lower quality of life; higher sum score correlates with better quality of life.

  8. Generic quality of life by SF36 [week 48]

    Short Form Health 36 (SF-36) shows health-related quality of life, 36 items in 8 categories, 25% of the items must be filled in per category for evaluation. Lower sum score correlates with lower quality of life; higher sum score correlates with better quality of life.

  9. Disease activity 2 by BHI [week 0]

    Harvey-Bradshaw Index - HBI is used to assess the degree of illness in individuals with Crohn's disease. The highest possible sum is 30 points and indicates a severe course of disease. A lower sum than 5 points indicates a clinical remission.

  10. Disease activity by HBI [week 12]

    Harvey-Bradshaw Index - HBI is used to assess the degree of illness in individuals with Crohn's disease. The highest possible sum is 30 points and indicates a severe course of disease. A lower sum than 5 points indicates a clinical remission.

  11. Disease activity by HBI [week 36]

    Harvey-Bradshaw Index - HBI is used to assess the degree of illness in individuals with Crohn's disease. The highest possible sum is 30 points and indicates a severe course of disease. A lower sum than 5 points indicates a clinical remission.

  12. Disease activity by HBI [week 48]

    Harvey-Bradshaw Index - HBI is used to assess the degree of illness in individuals with Crohn's disease. The highest possible sum is 30 points and indicates a severe course of disease. A lower sum than 5 points indicates a clinical remission.

  13. Anxiety and depression by HADS [week 0]

    Hospital Anxiety and Depression Scale (HADS), 14 items (7 each for depressive symptoms or symptoms of anxiety). The two summated scores of the summated scales HADS-A and HADS-D range between 0 and 21. high scores indicate depressivness and anxiety.

  14. Anxiety and depression by HADS [week 12]

    Hospital Anxiety and Depression Scale (HADS), 14 items (7 each for depressive symptoms or symptoms of anxiety). The two summated scores of the summated scales HADS-A and HADS-D range between 0 and 21. high scores indicate depressivness and anxiety.

  15. Anxiety and depression by HADS [week 36]

    Hospital Anxiety and Depression Scale (HADS), 14 items (7 each for depressive symptoms or symptoms of anxiety). The two summated scores of the summated scales HADS-A and HADS-D range between 0 and 21. high scores indicate depressivness and anxiety.

  16. Anxiety and depression by HADS [week 48]

    Hospital Anxiety and Depression Scale (HADS), 14 items (7 each for depressive symptoms or symptoms of anxiety). The two summated scores of the summated scales HADS-A and HADS-D range between 0 and 21. high scores indicate depressivness and anxiety.

  17. Perceived stress by PSS [week 0]

    Perceived Stress Scale (PSS), Rating on a five-step scale from 1 (=never) to 5 (=very often), high stress is assumed from a total score of 20 points

  18. Perceived stress by PSS [week 12]

    Perceived Stress Scale (PSS), Rating on a five-step scale from 1 (=never) to 5(=very often), high stress is assumed from a total score of 20 points

  19. Perceived stress by PSS [week 36]

    Perceived Stress Scale (PSS), Rating on a five-step scale from 1 (= never) to 5 (=very often), high stress is assumed from a total score of 20 points

  20. Perceived stress by PSS [week 48]

    Perceived Stress Scale (PSS), Rating on a five-step scale from 1 (= never) to 5 (=very often), high stress is assumed from a total score of 20 points

  21. Coping strategies by COPE [week 0]

    Coping Orientations to problems experienced Scale (COPE), total values of each scale vary between 2 (minimum) and 8 (maximum). Higher values indicate increased use of the specific coping strategy

  22. Coping strategies by COPE [week 12]

    Coping Orientations to problems experienced Scale (COPE), total values of each scale vary between 2 (minimum) and 8 (maximum). Higher values indicate increased use of the specific coping strategy

  23. Coping strategies by COPE [week 36]

    Coping Orientations to problems experienced Scale (COPE), total values of each scale vary between 2 (minimum) and 8 (maximum). Higher values indicate increased use of the specific coping strategy

  24. Coping strategies by COPE [week 48]

    Coping Orientations to problems experienced Scale (COPE), total values of each scale vary between 2 (minimum) and 8 (maximum). Higher values indicate increased use of the specific coping strategy

  25. Flourishing by FS-D [week 0]

    Flourishing Scale (FS-D), total value of the scale vary between 8 (minimum) and 56 (maximum). A high value corresponds to a person with many psychological resources and strengths.

  26. Flourishing by FS-D [week 12]

    Flourishing Scale (FS-D), total value of the scale vary between 8 (minimum) and 56 (maximum). A high value corresponds to a person with many psychological resources and strengths.

  27. Flourishing by FS-D [week 36]

    Flourishing Scale (FS-D), total value of the scale vary between 8 (minimum) and 56 (maximum). A high value corresponds to a person with many psychological resources and strengths.

  28. Flourishing by FS-D [week 48]

    Flourishing Scale (FS-D), total value of the scale vary between 8 (minimum) and 56 (maximum). A high value corresponds to a person with many psychological resources and strengths.

  29. Core Self-Evaluation by CSES [week 0]

    Core Self-Evaluation (CSES), 12 items on five-point Likert scale, 1 indicates disagreement and 5 indicates full agreement. High scores on the CSES represents a positive, confident, and self-efficacious person

  30. Core Self-Evaluation by CSES [week 12]

    Core Self-Evaluation (CSES), 12 items on five-point Likert scale, 1 indicates disagreement and 5 indicates full agreement. High scores on the CSES represents a positive, confident, and self-efficacious person

  31. Core Self-Evaluation by CSES [week 36]

    Core Self-Evaluation (CSES), 12 items on five-point Likert scale, 1 indicates disagreement and 5 indicates full agreement. High scores on the CSES represents a positive, confident, and self-efficacious person

  32. Core Self-Evaluation by CSES [week 48]

    Core Self-Evaluation (CSES), 12 items on five-point Likert scale, 1 indicates disagreement and 5 indicates full agreement. High scores on the CSES represents a positive, confident, and self-efficacious person

  33. CRP (C-reactive protein) [week 0]

    Determination of CRP in the blood

  34. CRP (C-reactive protein) [week 12]

    Determination of CRP in the blood

  35. CRP (C-reactive protein) [week 36]

    Determination of CRP in the blood

  36. CRP (C-reactive protein) [week 48]

    Determination of CRP in the blood

  37. BSG (blood cell sedimentation rate) [week 0]

    Determination of BSG in the blood

  38. BSG (blood cell sedimentation rate) [week 12]

    Determination of BSG in the blood

  39. BSG (blood cell sedimentation rate) [week 36]

    Determination of BSG in the blood

  40. BSG (blood cell sedimentation rate) [week 48]

    Determination of BSG in the blood

  41. creatinin [week 0]

    Determination of creatin in the blood

  42. creatinin [week 12]

    Determination of creatin in the blood

  43. creatinin [week 36]

    Determination of creatin in the blood

  44. creatinin [week 48]

    Determination of creatin in the blood

  45. lymphocyte (T-cell) profiling [week 0]

    Determination of lymphocyte (T-cell) profiling in the blood

  46. lymphocyte (T-cell) profiling [week 12]

    Determination of lymphocyte (T-cell) profiling in the blood

  47. lymphocyte (T-cell) profiling [week 36]

    Determination of lymphocyte (T-cell) profiling in the blood

  48. calprotectin [week 0]

    Determination of calprotectin in the stool

  49. calprotectin [week 12]

    Determination of calprotectin in the stool

  50. calprotectin [week 36]

    Determination of calprotectin in the stool

  51. calprotectin [week 48]

    Determination of calprotectin in the stool

  52. lactoferrin [week 0]

    Determination of lactoferrin in the stool

  53. lactoferrin [week 12]

    Determination of lactoferrin in the stool

  54. lactoferrin [week 36]

    Determination of lactoferrin in the stool

  55. lactoferrin [week 48]

    Determination of lactoferrin in the stool

  56. (PMN)-elastase [week 0]

    Determination of (PMN)-elastase in the stool

  57. (PMN)-elastase [week 12]

    Determination of (PMN)-elastase in the stool

  58. (PMN)-elastase [week 36]

    Determination of (PMN)-elastase in the stool

  59. (PMN)-elastase [week 48]

    Determination of (PMN)-elastase in the stool

  60. Human beta-defensin-2 (hBD-2) [week 0]

    Determination of hBD-2 in the stool

  61. Human beta-defensin-2 (hBD-2) [week 12]

    Determination of hBD-2 in the stool

  62. Human beta-defensin-2 (hBD-2) [week 36]

    Determination of hBD-2 in the stool

  63. Human beta-defensin-2 (hBD-2) [week 48]

    Determination of hBD-2 in the stool

  64. zonulin [week 0]

    Determination of zonulin in the stool

  65. zonulin [week 12]

    Determination of zonulin in the stool

  66. zonulin [week 36]

    Determination of zonulin in the stool

  67. zonulin [week 48]

    Determination of zonulin in the stool

  68. alpha-1-antitrypsin [week 0]

    Determination of alpha-antitrypsin in the stool

  69. alpha-1- antitrypsin [week 12]

    Determination of alpha-antitrypsin in the stool

  70. alpha-1-antitrypsin [week 36]

    Determination of alpha-antitrypsin in the stool

  71. alpha-1-antitrypsin [week 48]

    Determination of alpha-antitrypsin in the stool

  72. intestinal microbiome [week 0]

    Determination of intestinal microbiome

  73. intestinal microbiome [week 36]

    Determination of intestinal microbiome

  74. Intestinal permeability [week 0]

    confocal laser endomircoscopy

  75. cortisol [week 12]

    Determination of cortisol during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  76. ACTH [week 12]

    Determination of ACTH during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  77. prolactin levels [week 12]

    Determination of prolactin levels during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  78. glucocorticoid and β-adrenergic regulation of IL-8 and IL-10 [week 12]

    Determination of glucocorticoid and β-adrenergic regulation of IL-8 and IL-10 during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  79. TNF-α production by peripheral blood cells [week 12]

    Determination of TNF-α production by peripheral blood cells during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  80. heart rate [week 12]

    Determination of heart rate during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  81. blood pressure systolic and diastolic [week 12]

    Determination of blood pressure (systolic and diastolic) during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  82. STAI-S [week 12]

    Determination of STAI-S during Trier Social Stress Test at 4 points in time in the afternoon (right before, right after, 10 minutes after and 60 minutes after the Trier Social Stress Test)

  83. Adverse events [week 12]

    all adverse events

  84. Adverse events [week 36]

    all adverse events

  85. Adverse events [week 48]

    all adverse events

  86. qualitatives Interview [week 36]

    guideline oriented qualitative interview about the influence of the disease on the patients' everyday life, experience with the programme offered, effects of the intervention on the disease, implementation of the intervention in everyday life

  87. age (questionnaire) [week 0]

    age in years

  88. sex (questionnaire) [week 0]

    identification of the gender (male/female)

  89. weight [week 0]

    weight in kilograms

  90. body height [week 0]

    body height in meters

  91. School career (questionnaire) [week 0]

    identification of the school career

  92. job (questionnaire) [week 0]

    identification of the actual job

  93. professional career (questionnaire) [week 0]

    identification of job qualifications

  94. marital status (questionnaire) [week 0]

    identification of the marital status (married/divorced/single/widowed)

  95. occupation (questionnaire) [week 0]

    identification of the type of occupation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age between 18 and 75 years

  • Presence of a confirmed diagnosis of Crohn's disease

  • In remission (not longer than 12 months, or mild to moderate clinical activity (HBI <

  • Medication that has been stable for at least 3 months, regardless of whether glucocorticoids, immunosuppressive drugs, azathioprine, or other drug treatments according to MBMCrohn - Version 1.0 from 06.12.2019 Page 7 Guideline

  • Signed declaration of consent

Exclusion Criteria:
  • infectious or refractory Crohn's disease with severe course

  • Complete colectomy

  • Severe psychological illness (e.g. depression requiring treatment, addiction, schizophrenia)

  • Severe comorbid somatic disease (e.g. diabetes mellitus, oncological disease)

  • Pregnancy

  • Participation in stress reduction programmes or clinical studies on psychological interventions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sozialstiftung Bamberg, Klinik für Intergrative Medizin Bamberg Bayern Germany 96049

Sponsors and Collaborators

  • Jost Langhorst
  • Sozialstiftung Bamberg
  • University of Wuerzburg
  • Wuerzburg University Hospital
  • Bavarian State Ministry of Health and Care

Investigators

  • Study Director: Jost Langhorst, Prof., Sozialstiftung Bamberg

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jost Langhorst, Clinical Professor, Universität Duisburg-Essen
ClinicalTrials.gov Identifier:
NCT05182645
Other Study ID Numbers:
  • 19096
First Posted:
Jan 10, 2022
Last Update Posted:
Feb 4, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 4, 2022