The Effectiveness of Conservative Treatment in Patients With Complex Regional Pain Syndrome.

NCT07208825 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 156

Last updated 2025-10-06

No results posted yet for this study

Summary

The aim of the study is to investigate and improve non-pharmacological rehabilitation methods for patients with Complex Regional Pain Syndrome (CRPS) to reduce pain and restore work and functional capacity to lower overall treatment costs. Current treatment methods offer limited rehabilitation potential for this challenging pain condition, so efforts should be made to raise the level of care and rehabilitation for a disease that often causes long-term and severe reductions in patients' functional and occupational abilities. CRPS patients almost always have to substantially reduce their work hours or withdrawn from the workforce for extended periods, and often permanently, increasing the urgency of strengthening rehabilitation approaches; a CRPS symptoms can end a patient's productivity for society. In addition, commonly used medications are a significant expense for both individuals and the healthcare system. CRPS rarely resolves fully, and even with extensive rehabilitation only a small proportion of patients regain sufficient improvement to return to work at a level of at least 60% capacity.

Participants will be recruited from the Department of Physical Medicine and Rehabilitation at Oulu University Hospital, where CRPS diagnostics for the Northern Ostrobothnia area are primarily conducted. The study will be carried out at OYS rehabilitation outpatient clinics. A total of 39 participants will be recruited into each of four study groups, for an overall sample size of 156 individuals. Each study group will receive repetitive transcranial magnetic stimulation (rTMS) at some point, and functional neurological rehabilitation will be combined with rTMS in varying ways (content and timing will differ between groups). All participants will receive basic CRPS rehabilitation (physiotherapy and occupational therapy) that is provided for all RPS patients, and the timing of this relative to rTMS will also be varied. Recruitment is planned to begin in a autumn 2025.

Conditions

  • CRPS (Complex Regional Pain Syndromes)

Interventions

DEVICE

rTMS

2 weeks starting period (10 treatment days) followed by 5 treatment once a month.

OTHER

Basic physical therapy treatment

10 sessions with physical (or occupational) therapist with special education for treating CRPS

OTHER

Functional neurology

4 to 6 sessions with specialized OMT-physical therapist who will aim to improve the neurological deficits of the CRPS patient

DRUG

Optimizing the medication

Aim is to optimize the medication of the CRPS patient according the the medication guidelines

Sponsors & Collaborators

  • The Maud Kuistila Memorial Foundation

    collaborator UNKNOWN
  • Oulu University Hospital

    lead OTHER

Principal Investigators

  • Jani M Takatalo, PhD, MD, PRM Specialist · Oulu University Hospital, Pain Clinic

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-30
Primary Completion
2030-12-31
Completion
2033-12-31

Countries

  • Finland

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 NCT07208825 on ClinicalTrials.gov