The Rubber Hand Illusion (RHI) in Patients With CRPS

NCT ID: NCT01618578

Last Updated: 2012-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

69 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-05-31

Study Completion Date

2011-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The present study investigates by means of the rubber hand illusion body image stability and sense of body ownership in patients with CRPS of the upper limb compared to patients with unilateral pain of origin other than CRPS and age and sex-matched healthy subjects.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

In patients with CRPS of the upper limb distortions of body representation and impairments of sense of body ownership are well-known. To investigate the body schema and body image stability of these patients in comparison to patients with upper limb pain of origin other than CRPS and healthy subjects, we conducted a series of rubber hand illusions. This well - established paradigm is elicited by visuo-tactile stimulation of one´s own real hand and a visible hand and forearm prosthesis. The present study investigates 1) if and how far patients with CRPS are susceptible to experience the illusion 2) how far the illusion strength differs between CRPS and patients with unilateral pain of the upper limb of other origin and healthy subjects 3) how far parameters, e.g. neglect-like severity symptoms, body plasticity, empathy, duration of disease and pain intensity influence the illusion strength.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

CRPS Unilateral Limb Pain of Origin Other Than CRPS

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Patients with CRPS

24 patients with CRPS of the upper limb type 1 were included into the study.

rubber hand illusion

Intervention Type PROCEDURE

There were three consecutive trials of the RHI:

1. one control trial: asynchronous condition (3 Min.)
2. two experimental trials (conducted on both hands):synchronous condition (3 Min.),additionally watching the prosthesis being threatened (20 sec.)

Patients with unilateral upper limb pain

21 patients with unilateral upper limb pain served as controls.

rubber hand illusion

Intervention Type PROCEDURE

There were three consecutive trials of the RHI:

1. one control trial: asynchronous condition (3 Min.)
2. two experimental trials (conducted on both hands):synchronous condition (3 Min.),additionally watching the prosthesis being threatened (20 sec.)

healthy subjects

24 healthy subjects were age- and sex matched to patients with CRPS.

rubber hand illusion

Intervention Type PROCEDURE

There were three consecutive trials of the RHI:

1. one control trial: asynchronous condition (3 Min.)
2. two experimental trials (conducted on both hands):synchronous condition (3 Min.),additionally watching the prosthesis being threatened (20 sec.)

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

rubber hand illusion

There were three consecutive trials of the RHI:

1. one control trial: asynchronous condition (3 Min.)
2. two experimental trials (conducted on both hands):synchronous condition (3 Min.),additionally watching the prosthesis being threatened (20 sec.)

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

every participant:

* aged \> 18 years
* written informed consent
* free to withdraw participation at any time
* adequate understanding of the german language

Patients with CRPS:

* patients with CRPS type 1 of the upper limb
* clinical symptoms were diagnosed on the basis of the recently modified diagnostic research criteria (Harden, Bruehl et al., 2007)
* proved by typical enhancement in the late phase of the 99m-technetium-triple-phase bone skeleton scintigraphy (Wüppenhorst, Maier et al., 2010)

Patients with unilateral pain of the upper limb:

* unilateral pain
* pain of origin other than CRPS

Healthy subjects:

* age and sex matched to patients with CRPS
* checked by the DFNS IMI questionnaire

Exclusion Criteria

every participant:

* inadequate understanding of the german language
* missing informed consent
* diabetes mellitus

Patients with CRPS:

-CRPS Type 2
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ruhr University of Bochum

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Christoph Maier, Prof. Dr.

Prof. Dr. med. (Head of the pain clinic of the Bergmannsheil University Hospital)

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Christoph Maier, Prof. Dr.

Role: STUDY_DIRECTOR

Head of the pain clinic of the Bergmannsheil University Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Pain clinic of the Bergmannsheil University Hospital

Bochum, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RHI2010

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.