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Hypnotherapy for Prevention of Relapse in Ulcerative Colitis: a Randomised, Single-blind, Controlled Clinical Trial

Primary Purpose

Ulcerative Colitis

Status
Terminated
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Gut focussed hypnotherapy
Control educational sessions
Sponsored by
Queen Mary University of London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis focused on measuring Hypnotherapy, Prevention of relapse, ulcerative colitis

Eligibility Criteria

16 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Inactive UC
  • Age 16-75 years
  • Minimum 1 year on Azathioprine or Mercaptopurine.
  • Simple Colitis Activity Index (SCCAI) score <3
  • Baron's sigmoidoscopic score <2 .
  • In remission for at least 3 months
  • No change to other maintenance therapy (including 5ASA) for at least 4 months

Exclusion Criteria:

  • Use of prednisolone orally or topically, or of topical 5ASA for at least 3 months Antibiotics, warfarin, anti-diarrhoeal drugs, non-steroidal anti-inflammatory drugs (NSAIDs), aspirin > 75 mg/day
  • Herbal remedies
  • Alcohol or drug abuse
  • Pregnancy or breast feeding
  • Female of child-bearing age not taking adequate contraception
  • Participation in another drug trial in the previous three months
  • Serious liver, renal, cardiac, respiratory, endocrine, neurological or psychiatric illness
  • Already use relaxation techniques or computerized feedback

Sites / Locations

  • Barts and The Royal London NHS Trust/Queen Mary University London/
  • University College Hospital London
  • Guy's and St Thomas' NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Gut-focussed hypnotherapy (GFH).

Educational sessions

Arm Description

Gut-focussed hypnotherapy (GFH).

Regular sessions to learn about UC from research nurse

Outcomes

Primary Outcome Measures

Relapse at 1 Year
The number of patients suffering a relapse was compared between the two treatment groups, and was the primary outcome parameter of this study.

Secondary Outcome Measures

Inflammatory Bowel Disease Questionnaire (IBDQ) at Week 13
IBDQ (standard measure of IBD patients' Quality of life (QoL) (Irvine et al 1982 approx). The IBDQ is a validated and reliable tool to measure of health-related quality of life in adult patients with IBD. The questionnaire consists of 32 questions scored in four domains: bowel symptoms, emotional health, systemic systems and social function. Scores range from 1 (poorest QoL) to 7 (best QoL). Higher scores indicate better QoL. Lowest score 7, highest score 224.
Hospital Anxiety and Depression Score-Anxiety, (HADSA) at Week 13
Measure of anxiety, HADS Hospital anxiety and depression scale. HADS questionnaire consists of a 14 question validated questionnaire, developed to measure anxiety and depression in the hospital setting. Each item is answered by the patient on a four point (0-3) response category so the possible scores range from 0 (minimum) to 21 (maximum) for anxiety and 0 (minimum) to 21 (maximum) for depression. Higher scores indicate worse outcome,
Hospital Anxiety and Depression Score-Depression (HADSD)
Measure of depression. Each item is answered by the patient on a four point (0-3) response category so the possible scores range from 0 to 21 for anxiety and 0 to 21 for depression. Each item is answered by the patient on a four point (0-3) response category so the possible scores range from 0 (minimum) to 21 (maximum) for anxiety and (minimum) to 21 (maximum) for depression. Higher scores worse outcome.
Perceived Stress Questionnaire-Recent (PSQ-R)
Measure of recent psychological stress. THE PSQ R consists of a 30 question questionnaires: recent, in which the statements used apply to the last month in which used statements apply to the last two years (Appendix 1.3). The score for both recent and general stress levels were stated as the PSQ index ranging from 0 (non-stressed) to 0.99 (highly stressed). Higher scores indicate worse outcome.

Full Information

First Posted
November 2, 2007
Last Updated
April 2, 2019
Sponsor
Queen Mary University of London
Collaborators
Barts & The London NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00553163
Brief Title
Hypnotherapy for Prevention of Relapse in Ulcerative Colitis: a Randomised, Single-blind, Controlled Clinical Trial
Official Title
Hypnotherapy for Prevention of Relapse in Ulcerative Colitis: a Randomised, Single-blind, Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Terminated
Why Stopped
Unable to recruit sufficient numbers of patinets in the time available
Study Start Date
October 2007 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Queen Mary University of London
Collaborators
Barts & The London NHS Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There is increasing evidence that worsening of ulcerative colitis (UC) can be provoked by psychological stresses. When this protocol was devised, there had been no proper scientific studies to find out whether stress reduction can improve the course of UC. Hypnotherapy is a technique by which a practitioner induces a temporary trance-like state in patients: while they are in this state, the practitioner uses suggestion to induce relaxation as well as beneficial modification of the way in which the patient experiences the gut working. In previous studies in our lab, we have shown that a single 50 minute session of hypnosis can reduce special indicators of inflammation both in the blood-stream and in the lining of the lower bowel (rectum). Furthermore, in earlier work by others, hypnosis had been shown to be effective in the treatment of patients with irritable bowel syndrome, duodenal ulcer and indigestion unassociated with ulcers. Many patients with UC need to take the immunosuppressive drug, azathioprine, in addition to a 5ASA drug, to keep their disease under control. While azathioprine is usually effective in maintaining remission of UC, it does require regular drug checks and carries the risk of possible side-effects. We undertook a study of hypnotherapy to see whether it can prevent relapse (worsening) of UC in patients who normally need to take azathioprine to keep their UC inactive. To do this, we planned to ask 66 patients who agreed to participate in the trial to stop their azathioprine. They were then to be allocated to receive either gut-focussed hypnotherapy (44 patients) or, as a control, non-emotive educational sessions (22 patients) once a month for 3 months, with intervening self-hypnosis daily in the active arm. The numbers of patients in each group who developed relapse of their UC in a year were recorded. We diagnosed relapse from patients' diaries recording diarrhoea and bleeding, and by sigmoidoscopy. It was hoped that this clinical trial would identify a new drug-free way of reducing the chances of relapse in patients with UC.
Detailed Description
SCIENTIFIC ABSTRACT There is increasing evidence that relapse of ulcerative colitis (UC) can be provoked by psychological stress. When this study was planned, there were no proper scientific studies to find out whether stress reduction can improve the course of UC. Hypnotherapy is a technique by which a practitioner induces a temporary trance-like state in patients: while they are in this state, the practitioner uses suggestion to induce relaxation as well as beneficial modification of the way in which the patient experiences the gut working. In previous studies in our lab, we had shown that a single session of hypnosis can reduce measures of inflammation at both systemic and rectal mucosal levels. Thus, 50 min of gut-focussed hypnosis reduced serum interleukin-6 (IL6) and non-killer (NK) cell numbers in circulating blood, as well as rectal mucosal release of interleukin-13 (IL13), substance P and histamine. Furthermore, in earlier work by others, hypnosis had been shown to be effective in the treatment of patients with irritable bowel syndrome, duodenal ulcer and indigestion unassociated with ulcers. Many patients with UC need to take the immunosuppressive, azathioprine, in addition to a 5ASA, to keep their disease in remission. While azathioprine is usually effective in maintaining remission of UC, it does require regular drug checks and carries the risk of possible side-effects. We undertook a study of hypnotherapy to see whether it could prevent relapse of UC in patients who normally need to take azathioprine to keep their UC inactive. To do this, we planned to ask 66 patients who agreed to participate in the trial to stop their azathioprine. They were then to be allocated to receive either gut-focussed hypnotherapy (44 patients) or, as a control, non-emotive educational sessions (22 patients) once a month for 3 months, with intervening self-hypnosis daily in the active arm. We then recorded relapse rates in each group at 1 year. We diagnosed relapse from patients' diaries recording the Simple Clinical Activity Index, and by Baron score >1 at sigmoidoscopy. It was hoped that this clinical trial would identify a new drug-free way of reducing the chances of relapse in patients with UC withdrawing from treatment with azathioprine.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
Keywords
Hypnotherapy, Prevention of relapse, ulcerative colitis

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Gut-focussed hypnotherapy (GFH).
Arm Type
Active Comparator
Arm Description
Gut-focussed hypnotherapy (GFH).
Arm Title
Educational sessions
Arm Type
Sham Comparator
Arm Description
Regular sessions to learn about UC from research nurse
Intervention Type
Behavioral
Intervention Name(s)
Gut focussed hypnotherapy
Intervention Description
Gut focussed hypnotherapy
Intervention Type
Behavioral
Intervention Name(s)
Control educational sessions
Intervention Description
Control educational sessions
Primary Outcome Measure Information:
Title
Relapse at 1 Year
Description
The number of patients suffering a relapse was compared between the two treatment groups, and was the primary outcome parameter of this study.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Inflammatory Bowel Disease Questionnaire (IBDQ) at Week 13
Description
IBDQ (standard measure of IBD patients' Quality of life (QoL) (Irvine et al 1982 approx). The IBDQ is a validated and reliable tool to measure of health-related quality of life in adult patients with IBD. The questionnaire consists of 32 questions scored in four domains: bowel symptoms, emotional health, systemic systems and social function. Scores range from 1 (poorest QoL) to 7 (best QoL). Higher scores indicate better QoL. Lowest score 7, highest score 224.
Time Frame
13 weeks
Title
Hospital Anxiety and Depression Score-Anxiety, (HADSA) at Week 13
Description
Measure of anxiety, HADS Hospital anxiety and depression scale. HADS questionnaire consists of a 14 question validated questionnaire, developed to measure anxiety and depression in the hospital setting. Each item is answered by the patient on a four point (0-3) response category so the possible scores range from 0 (minimum) to 21 (maximum) for anxiety and 0 (minimum) to 21 (maximum) for depression. Higher scores indicate worse outcome,
Time Frame
13 weeks
Title
Hospital Anxiety and Depression Score-Depression (HADSD)
Description
Measure of depression. Each item is answered by the patient on a four point (0-3) response category so the possible scores range from 0 to 21 for anxiety and 0 to 21 for depression. Each item is answered by the patient on a four point (0-3) response category so the possible scores range from 0 (minimum) to 21 (maximum) for anxiety and (minimum) to 21 (maximum) for depression. Higher scores worse outcome.
Time Frame
13 weeks
Title
Perceived Stress Questionnaire-Recent (PSQ-R)
Description
Measure of recent psychological stress. THE PSQ R consists of a 30 question questionnaires: recent, in which the statements used apply to the last month in which used statements apply to the last two years (Appendix 1.3). The score for both recent and general stress levels were stated as the PSQ index ranging from 0 (non-stressed) to 0.99 (highly stressed). Higher scores indicate worse outcome.
Time Frame
13 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Inactive UC Age 16-75 years Minimum 1 year on Azathioprine or Mercaptopurine. Simple Colitis Activity Index (SCCAI) score <3 Baron's sigmoidoscopic score <2 . In remission for at least 3 months No change to other maintenance therapy (including 5ASA) for at least 4 months Exclusion Criteria: Use of prednisolone orally or topically, or of topical 5ASA for at least 3 months Antibiotics, warfarin, anti-diarrhoeal drugs, non-steroidal anti-inflammatory drugs (NSAIDs), aspirin > 75 mg/day Herbal remedies Alcohol or drug abuse Pregnancy or breast feeding Female of child-bearing age not taking adequate contraception Participation in another drug trial in the previous three months Serious liver, renal, cardiac, respiratory, endocrine, neurological or psychiatric illness Already use relaxation techniques or computerized feedback
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David S Rampton, MAFRCP DPhil
Organizational Affiliation
Barts and the London/Queen Mary School of Medicine and Dentistry, London.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anton Emmanuel, MBBS MD FRCP
Organizational Affiliation
University College London Hospital, London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Louise Langmead, MBBS MD MRCP
Organizational Affiliation
Univesity College London Hospital , London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jeremy D Sanderson, MBBSFRCP MD
Organizational Affiliation
Guy's and St Thomas'NHS Trust/King's College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Barts and The Royal London NHS Trust/Queen Mary University London/
City
London
ZIP/Postal Code
E1 1BB
Country
United Kingdom
Facility Name
University College Hospital London
City
London
ZIP/Postal Code
NW1 2BU
Country
United Kingdom
Facility Name
Guy's and St Thomas' NHS Trust
City
London
ZIP/Postal Code
SE1 7EH
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
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Hypnotherapy for Prevention of Relapse in Ulcerative Colitis: a Randomised, Single-blind, Controlled Clinical Trial

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