Self-rehabilitation At Home After LumbaR Arthrodesis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Lumbar arthrodesis is more and more common in general population. Patients need early reeducation after surgery but do not always have access to a physiotherapist. The investigators aim to study the benefits of self-rehabilitation at home after lumbar arthrodesis, showing amelioration in lumbar pain and in quality of life for concerned patients. For this, the investigators designed a randomized-controlled study to test if self-rehabilitation at home right after surgery is superior than rehabilitation done by a physiotherapist 4 to 6 weeks after surgery (standard treatment for our patients).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Lumbar pain and/or nerve root pain and/or limp without any motor deficiency of the limbs, before and/or after surgery (if any motor deficiency occurs after surgery, it will be a secondary exclusion criteria)

• Surgery for posterolateral lumbar arthrodesis, from a degenerative etiology, from 1 to 3 lumbar levels (one level means one inter-somatic space)

• Surgery indication after optimal medical treatment, including appropriate pain medicine, and fail of medical treatment for reducing lumbar pain and/or nerve root pain and/or limp

• Return home possible after surgery

• After signing consent during pre-operative visit with the surgeon

Locations
Other Locations
France
AP-HP - Hôpital Européen Georges-Pompidou Paris, France
RECRUITING
Paris
Contact Information
Primary
Breno MELO, PhD
gestion-locale.drc@aphp.fr
(0)140271988
Backup
Youcef Sekour
youcef.sekour@aphp.fr
Time Frame
Start Date: 2023-12-18
Estimated Completion Date: 2028-10
Participants
Target number of participants: 120
Treatments
No_intervention: Standard of care
Experimental: Self rehabilitation at home
Related Therapeutic Areas
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov