Skip to content

The effect of Eye Movement Desensitisation and Reprocessing (EMDR) on abdominal pain in patients with Irritable Bowel Syndrome (IBS).

The effect of Eye Movement Desensitisation and Reprocessing (EMDR) on abdominal pain in patients with Irritable Bowel Syndrome (IBS). - EMDR for IBS

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49387
Enrollment
34
Registered
2020-05-29
Start date
2020-11-30
Completion date
Unknown
Last updated
2024-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritable Bowel Irritable Bowel Syndrome

Interventions

Patients in de treatment condition (after intake/case conceptualization) receive 6 weekly sessions of EMDR treatment (each 90 lasting minutes).

Sponsors

Diakonessenhuis Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult (18-65 yrs old) Meets ROME IV criteria for Irritable Bowel Syndrome Severe and frequent abdominal pain (as measured by Irritable Bowel Syndrome-Severity Scoring System).

Exclusion criteria

Exclusion criteria: Insufficient knowlegde of Dutch language (to fill out questionnaires, or for communication) Psychiatric problems that demand immediate treatment Ongoing treatment for psychotrauma. Somatic disorders that cause abdominal pain such as Colitis and Crohn's disease. Substance abuse

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is the severity of the abdominal pain as measured by diary registration. At all three measuring times (T1, T2, T3), during two weeks, patients are asked to rate their abdominal pain on a Likert scale (0-10). The calculated mean over all rated days will be used as primary outcome measure.

Secondary

MeasureTime frame
* Severity of IBS complaints 1) diary measurements like described above for pain are taken for two other IBS complaints (specifically, the two most troublesome IBS complaints). The calculated mean over all rated days will be used as outcome measure. 2) total score on the Irritable Bowel Syndrome-Severity Scoring System * Quality of Life 1) at T1, T2 and T3 diary measurements patients are asked to rate the burden they experience due to their IBS complaints in two valued activities (Likert scale 0-10). The calculated mean over all rated days will be used as outcome measure. 2) total score on the Irritable Bowel Syndrome- Quality of Life measure. * Experienced relief of complaints - Adequate Relief Question

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)