MedPath

Shared Responsibility Between General Practitioners and Highly Specialized Hospitals in Spinal Cord Injury

Not Applicable
Conditions
Spinal Cord Injuries
Registration Number
NCT04071938
Lead Sponsor
Schweizer Paraplegiker Forschung
Brief Summary

It is an interventional study that aims to assess a new primary care model of collaboration between specialized centers and primary care physicians in Switzerland, in order to reduce morbidity and improve patients' and providers' experience with delivery of follow-up care in individuals with chronic spinal cord injury as compared to current best practice.

Detailed Description

This model will lead to awareness, recognition and interactive communication between GPs and specialists and guidelines on the shared-role relationship.

The study interventions are educational modules on bladder, bowel, skin-care, and pain management which will be provided to participating GPs by Spinal Cord Injury specialists. In addition visits by specialized nurses to the participating GPs at their practices to support the establishment of specialized care on-site.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
273
Inclusion Criteria

Physicians

  • GPs practicing in medium to large group practice
  • The practice is wheelchair accessible and remote to SCI specialized centers
  • Proficiency certificate in ultrasonography

Patients:

  • Diagnosed with traumatic or non-traumatic, sensory or motor complete or incomplete, chronic SCI
  • 18 years or older
  • Permanently reside in Switzerland
  • Reside farther than 25 minutes driving distance from a specialized SCI center
  • Understand German, English, Italian
  • Informed consent
  • Additionally in treatment group: Patients with chronic SCI Living in the region of a participating GP irrespective if they visit the participating primary care practice.
  • Additionally in control group: individuals with SCI who live outside the catchment areas
Exclusion Criteria

Patients:

  • Acute SCI or during first rehabilitation phase - Congenital conditions leading to paraplegia or tetraplegia, including spina bifida - Neurodegenerative disorders such as multiple sclerosis and amyotrophic lateral sclerosis - Guillain-Barré syndrome

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Average difference in total score of Doctor's Opinions on Collaboration (DOC)Change from baseline to 12 and 24 months post intervention

DOC is a validated questionnaire covering organization, communication, professional expertise, image and knowing each other. It will be completed by GPs and SCI specialists. The DOC will be converted to an interval score and scaled from 0 to 100 with minimum and maximum score (0=completely agree, 100=completely disagree)

Average difference in total score of Modified Spinal Cord Injury Secondary Conditions Scale (SCI-SCS) scoreChange from baseline to 12 and 24 months post intervention

Modified Spinal Cord Secondary Conditions Scale (SCI-SCS) targets secondary conditions associated with SCI composite endpoint, excluding diabetes mellitus and joint and muscle pain. Modified (SCI-SCS) includes 14 health conditions and chronic pain. Self reporting through questionnaires on pressure sores, urinary tract infections, spasticity, postural hypotension, bowel, and bladder problems, etc...). The rating scale uses a 4-point ordinal scale ranging from 0 (not experienced/insignificant problem never limiting activity) to 3 (significant/chronic problem).

Secondary Outcome Measures
NameTimeMethod
Average difference in number of patients visits to a specialist or a SCI centerChange from baseline to 12 and 24 months post intervention

Number of visits to SCI specialist of SCI center people with SCI had in 12 months period

Average difference in subscore on UTIsChange from baseline to 12 and 24 months post intervention

from Modified Spinal Cord Injury Secondary Conditions Scale (SCI-SCS)Subscore on urinary tract infections (UTIs) with a 4-point rating on severity, ranging from 0 (not experienced/insignificant problem never limiting activity) to 3 (significant/chronic problem)

Average difference in the number of inpatient hospitalizationChange from baseline to 12 months and 24 months post intervention

Number of hospitalizations people with SCI had in 12 months period

Physicians' satisfactionChange in overall satisfaction scores from baseline to 12 and 24 months post intervention

Questionnaire distributed to physicians in intervention and control group to measure the difference in the satisfaction with the collaboration between the health care providers.

Average difference in subscore on pressure soresChange from baseline to 12 and 24 months post intervention

from Modified Spinal Cord Injury Secondary Conditions Scale (SCI-SCS)Subscore on pressure sores with a 4-point rating on severity, ranging from 0 (not experienced/insignificant problem never limiting activity) to 3 (significant/chronic problem)

Trial Locations

Locations (1)

Schweizer Paraplegiker Forschung

🇨🇭

Nottwil, Luzern, Switzerland

Schweizer Paraplegiker Forschung
🇨🇭Nottwil, Luzern, Switzerland

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.