The relation between somatosensation, nociception and the development of shoulder pain after stroke.

The relation between somatosensation, nociception and the development of shoulder pain after stroke. - The development of shoulder pain after stroke

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON33220

Enrollment

100

Registered

2009-04-29

Start date

2009-05-19

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

cerebro vacular accident Stroke

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Older than 18 years, legally competent, able to communicate, first-ever unilateral CVA (ischemic or hemorrhagic) of the middle cerebral artery (if possible confirmation by CT or MRI scan), somatosensory and motor loss during baseline measurement (0-2 weeks after stroke), sign informed consent

Exclusion criteria

Exclusion criteria: Pregnancy, HIV/AIDS, any other brain disease (trauma, tumor, parkinson, multiple sclerosis), any peripheral neurological disease (amputation, neuropathy), pre-existent psychiatric disorders, pre-existent use of psychotropic substances or medication, chronic pain complaint (> 3 subsequent months) in the 6 months prior to stroke

Design outcomes

Primary

Measure	Time frame
Baseline assessment consists of the assessment of pain complaints (current, past) and assessment of neurological function. Follow-up measurements consist of the assessment of pain complaints (quality, quantity) and the assessment of somatosensory and nociceptive changes using quantitative sensory testing and cold pressor testing.	—

Secondary

Measure	Time frame
x	—

Countries

Netherlands

Outcome results