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Physical and Psychological Changes in CRPS Patients Undergoing Multimodal Rehabilitation

NCT05696587 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2023-11-15

No results posted yet for this study

Summary

The goal of this clinical trial is to learn about cognitive changes during rehabilitation in CRPS patients. The main questions it aims to answer are:

* What are the cognitive changes in CRPS?
* Do cognitive functions change during multimodal rehabilitation in CRPS?
* What is the effect of multimodal rehabilitation on pain, functioning, mood, active range of motion, cognitive functions.

Participants will undergo a 4-week program of multimodal rehabilitation of physical therapy, education and Graded Motor Imagery. Assessment will be made at baseline and after 4 weeks.

Researchers will compare the interventional arm with healthy control to see if the observed psychological results are exclusive to CRPS group.

There is no expanded access scheduled for this study.

Conditions

  • Complex Regional Pain Syndromes

Interventions

OTHER

Multimodal rehabilitation

The multimodal rehabilitation program included comprehensive therapy 5 times a week during the 4 weeks between assessments. The therapy consists of: * Individual physical therapy focused on improving range of motion and alleviating pain in the affected limb; * Mechanical desensitization; * Transcutaneous electric nerve stimulation (TENS) electrotherapy; * Aquatherapy (arm or leg whirlpool bath of the affected extremity); * Graded Motor Imagery, including the Recognise™ app and mirror therapy; * Psychoeducation on relaxation and coping with chronic pain.

Sponsors & Collaborators

  • National Institute of Geriatrics, Rheumatology and Rehabilitation, Poland

    lead NETWORK

Principal Investigators

  • Beata Tarnacka, ASSC PROF · National Institute of Geriatrics, Rheumatology and Rehabilitation

  • Adam Zalewski, MD · National Institute of Geriatrics, Rheumatology and Rehabilitation

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-10-10
Primary Completion
2023-01-20
Completion
2023-02-01

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05696587 on ClinicalTrials.gov