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Neurophysiological Basis of Rehabilitation in Patients with Complex Regional Pain Syndrome-Type I (CRPS-I) and chronic Low Back Pain (LBP)

Neurophysiological Basis of Rehabilitation in Patients with Complex Regional Pain Syndrome-Type I (CRPS-I) and chronic Low Back Pain (LBP) - Neural correlates of rehabilitation in CRPS-I and LBP patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON41326
Enrollment
75
Registered
2012-02-29
Start date
2015-01-19
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

chronic pain syndromes Complex Regional Pain Syndrome type I (CRPS-I) and chronic pain

Interventions

None listed

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: for CRPS-I patients: - Diagnosis of Complex Regional Pain Syndrome Type I - Unilateral localization on upper extremity;for LBP patients: - Experience of non-specific low back pain for at least three months - No other diagnosis better explaining the signs and symptoms;all patients: - Stable medication - Substantial fear of movement/(re)-injury;for all patients and healthy controls: - Age between 18 and 65 years old

Exclusion criteria

Exclusion criteria: for patients and healthy controls: - peripheral neuropathy of upper extremity - magnetic resonance imaging incompatible health condition - psychopathology (according to SCL 90) - tactile sensitivity impairment as a result of cranial, spinal lesion or damage of sensory apparatus for healthy controls only: - (history of) CRPS or other chronic pain syndromes

Design outcomes

Primary

MeasureTime frame
Patients and healthy controls: 1) Blood-oxygenation level dependent response (BOLD signal), during rest, during the tactile stimulations and during watching of pictures that might be experienced as threatful by the patients. 2) Tactile discrimination threshold in mm (minimal offset in dot pattern required for reliable discrimination [>80%] of the directionality of this offset)(CRPS-I) / Performance on lifting task (LBP) 3) Fractional anisotropy of water diffusivity.

Secondary

MeasureTime frame
patients and healthy controls: - Pain feedback during MRI session - Handedness as measured by the Edinburgh handedness inventory. - Physical activity in daily life measured during 7 days around the pre and post measurement with the Actiwatch motion sensor (Cambridge Neurotechnology Ltd., Cambridge, UK) on the left and right arm. - Fear of movement, measured by three standard questionnaires : the Tampa Scale for Kinesiophobia, the Photograph series of daily activities for the upper extremities (PHODA-UE), the Pain Anxiety Symptoms Scale (PASS-20). - Catastrophic thinking, measured by the Pain Catastrophizing Scale. - Bodily structure and function, measured by: 1. the Neuropathic Pain Scale; 2. the McGill Pain Questionnaire Dutch version (MPQ-DLV); 3. Aβ-fibre mediated allodynia for the upper extremities. 4. Vasomotoric symptoms: temperature differences; 5. Sudomotoric symptoms: edema. patients only: - Dairy measurements of the symptoms measured by some items from the above mentioned questionnaires. Other parameters patients and healthy controls: - Demographic characteristics patients only: - Illness-related facts (duration, localisation etc.) - Compliance and involvement, as indicated by treatment session attendance and completed diary entries.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)