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Evaluation and Timing in an ERAS-like Structured Rehabilitation Program After Lumbar Spine Surgery

NCT05937997 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 245

Last updated 2023-07-10

No results posted yet for this study

Summary

The goal of this clinical trial is to investigate the safety of early inpatient rehabilitation after lumbar spine surgery.

Participants are assigned to therapy groups C (low) - A (high) intensity and receive standardized multimodal rehabilitation for 3 weeks. Groups are compared in terms of safety, disability impairment as well as pain. Timing of rehabilitation is considered.

Conditions

  • Lumbar Pain Syndrome

Interventions

PROCEDURE

high intensity physiotherapy

high intensity exercises for 3 weeks inpatient rehabilitation

PROCEDURE

moderate intensity physiotherapy

moderate intensity exercises for 3 weeks inpatient rehabilitation

PROCEDURE

low intensity physiotherapy

low intensity exercises for 3 weeks inpatient rehabilitation

Sponsors & Collaborators

  • Johannes Gutenberg University Mainz

    collaborator OTHER

  • Median

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-29
Primary Completion
2016-11-21
Completion
2016-11-21

Countries

  • Germany

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 NCT05937997 on ClinicalTrials.gov