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Investigating the effect of Eye Movement Desensitization and Reprocessing (EMDR) on fibromyalgia: a ten times replicated multiple-baseline experimental case study

Investigating the effect of Eye Movement Desensitization and Reprocessing (EMDR) on fibromyalgia: a ten times replicated multiple-baseline experimental case study - EMDR4FM

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50804
Enrollment
10
Registered
2021-09-28
Start date
2022-01-20
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

chronic pain syndrome Fibromyalgia

Interventions

EMDR therapy consists of seven sessions of 90 minutes in total, performed according to the EMDR standard protocol. EMDR focuses on processing traumatic memories and pain-related memories.

Sponsors

GGZ Noord-Holland-Noord
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) a medical diagnosis of fibromyalgia 2) age of 18 years and older 3) an average pain intensity score in the past week of >= 7 on a Numerical Rating Scale for Pain 4) sufficient understanding of the Dutch language verbally and in writing, in order to be able to participate 5) willingness to participate in the study (as indicated by the signed informed consent)

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1) an acute condition of psychosis or bipolar disorder 2) an acute suicidal risk 3) an IQ

Design outcomes

Primary

MeasureTime frame
Daily data are collected of the primary parameter which is pain intensity.

Secondary

MeasureTime frame
Secondary parameters are stiffness in muscles and joints, fatigue, the impact of pain on daily life, the impact of pain on sleep and a selection of four PTSD symptoms. Exploratory analysis: At specific time points data will be collected of the impact of FM complaints on daily life, PTSD symptoms, psychiatric symptoms and functioning in general, depressive symptoms, central sensitization symptoms and the patient impression of change. The time points are at the start of the baseline, at the end of the baseline period which corresponds to the start of the intervention, directly after the EMDR treatment, one month after the EMDR treatment and three months after the EMDR treatment.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)