Skip to main content
Clinical Trials/NL-OMON53643
NL-OMON53643
Not Yet Recruiting
N/A

Affective touch; reducing pain in Parkinson patients study 2 - Affective touch; reducing pain in Parkinson patients study 2

niversiteit Utrecht0 sites34 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronische pijn bij Parkinson
Sponsor
niversiteit Utrecht
Enrollment
34
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • In order to be eligible to participate in this study, a participant must meet
  • all of the following criteria:
  • \- Age \>\=18
  • \- Diagnosed with PD, confirmed by Het Diakonessenhuis department of neurology
  • or St. Antonius Hospital department of neurology
  • \- Pain associated with PD (musculoskeletal, dystonic, akathisia) and pain
  • worsened by PD (i.e. (osteo)arthritis or other age\-related pain conditions)
  • \- Pain must be present for at least 3 months, with clear impact on
  • physical/psychological functioning, which must be assessed as at least moderate
  • in intensity (\>\=4 points on the BPI).

Exclusion Criteria

  • A potential participant who meets any of the following criteria will be
  • excluded from participation in this study:
  • \- Incapability of giving informed consent. To assess whether participants are
  • able to give informed consent the token test will be used. The token test is
  • used to assess language comprehension, if participants score below the cut\-off
  • score this may point to language comprehension problems which could alter their
  • decision making and ability to provide informed consent, in which case
  • participants are excluded from participation.
  • \- Incapability of interpreting questionnaires, the token test will also be used
  • to assess the capability of interpreting the questionnaires.

Outcomes

Primary Outcomes

Not specified

Similar Trials