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Clinical Trials/NCT06129682
NCT06129682RecruitingNot Applicable

Self-rehabilitation At Home After LumbaR Arthrodesis

Assistance Publique - Hôpitaux de Paris1 site in 1 country120 target enrollmentStarted: December 18, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
120
Locations
1
Primary Endpoint
Change of lumbar pain

Study Overview

Brief 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).

Detailed Description

Due to population aging, lumbar arthrodesis is becoming more frequent in general population. At the same time, those patients need early rehabilitation, even if they do not experiment any motor disability after surgery : it has been showed that early rehabilitation improves lumbar pain thanks to muscle strengthening.

The design of the study is prospective,monocentric, controlled and randomized. This study compares progressive self-rehabilitation at home after lumbar arthrodesis, explained to the patient by a physiotherapist during his or her stay at the hospital and started right after surgery, versus rehabilitation done by a physiotherapist 4 to 6 weeks after surgery (standard treatment).

The primary outcome is decrease of lumbar pain at 6 weeks and 3 months after surgery. The secondary outcomes are improvement of functional abilities and improvement of pelvis and limbs ranges of motion.

Patients of both groups will be followed by surgeon and physiotherapist at 6 weeks and 3 months.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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
  • •Exclusion Criteria:
  • •People under 18 years-old
  • •Pregnant or breast-feeding women
  • •Psychiatric and/or neurodegenerative comorbidity
  • •Motor deficiency of the limbs before and/or after surgery
  • •Iliac extension of arthrodesis
  • •Any postoperative complication lengthening stay at hospital
  • •Medical contraindication for early rehabilitation

Arms & Interventions

Standard of care

No Intervention

Self rehabilitation at home

Experimental

Intervention: Self rehabilitation at home (Other)

Outcomes

Primary Outcomes

Change of lumbar pain

Time Frame: At 6 weeks and 3 months after surgery

Improvement of Short Form 36 score (SF-36) Unit : number of points Each item is graded on a scale of 0 to 100, with 0 and 100 serving as the lowest and highest possible scores. A higher number indicates that the subject is in better overall health.

Secondary Outcomes

  • Improvement of ranges of motion - Ely test(At 6 weeks and 3 months after surgery)
  • Improvement of ranges of motion - Straight Leg Test(At 6 weeks and 3 months after surgery)
  • Improvement of ranges of motion - Schober test(At 6 weeks and 3 months after surgery)
  • Improvement of functional abilities(At 6 weeks and 3 months after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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