Effects of a Single Session of Physiotherapy on Patients Operated for Lumbar Spondylolisthesis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorIstituto Clinico Humanitas

About this trial

The goal of this clinical trial is to investigate whether a meeting with physiotherapist before hospital discharge can improve the post-operative outcomes in patients who have undergone lumbar fusion surgery for spondylolisthesis.

The main question it aims to answer is:

* The primary endpoint investigated is the degree of disability measured using the ODI-I one month after the surgical intervention. * The secondary endpoints are the level of pain measured using the NRS scale at 1 and 3 months post-surgery; disability at 3 months measured using the ODI-I questionnaire; physical function assessed using the UWT at 1 and 3 months post-surgery; psychological factors such as self-efficacy and fear of movement measured using the TSK and PSEQ-I at 1 and 3 months after lumbar fusion surgery; health status and quality of life measured at 3 months with the HADS-I and SF-36-I questionnaires; and the patient's satisfaction regarding their hospital stay, assessed using a PREMs questionnaire administered at the time of discharge.

The "usual care" group will instead be discharged by the spinal surgeon following the standard procedures.

The physiotherapist will provide the patient with advice regarding their return home and will suggest simple exercise to be performed at home until the next visit, one month after surgery. Additionally, the patient will have the opportunity to communicate, either by email or phone, with the physiotherapist until the follow-up visit with the spinal surgeon.

Eligibility criteria

Qualifiers

Age > 18 years

Patients who have undergone lumbar fusion surgery due to monosegmental lumbar spondylolisthesis.

Disqualifiers

Patients who have undergone previous lumbar surgeries

Patients operated on for other lumbar pathologies

Patients with pre-existing neurological deficits not related to the condition being treated

Patients with systemic conditions (inflammatory, infectious, neoplastic, etc.) or neuromuscular disorders

Trial design

Treatments tested in this trial

  • Education
  • Usual Care

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators