eg Variables During Surgical Recovery Period In Patients With Cervical Spondylotic Myelopathy

Not Applicable

• Conditions: Health Condition 1: G55- Nerve root and plexus compressionsin diseases classified elsewhere

• Registration Number: CTRI/2022/08/044841
• Lead Sponsor: FERNANDES TANYA DAISY

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Inclusion criteria for Cervical Spondylotic Myelopathy patients:

1. Patients diagnosed with Cervical Spondylotic Myelopathy by a qualified neurosurgeon/

Neurologist undergone surgical decompression (anterior or posterior approach)

2. Patients post operative duration of 4-6 weeks

3. Patients well oriented

4. Patients of both genders

5. Patients with grade 0 to 3 on Modified Nurick grading for cervical myelopathy35

6. Patients in 40- 60 years of age group

7. Patients able to understand and follow commands

8. Patients who are able to independently perform posture transitions, maintain static standing

� Inclusion criteria for aged and gender matched normative participants:

1. Participants in 40 to 60 years of age

2. Participants of both genders included

3. Patients who are able to independently perform posture transition, maintain static standing

Exclusion Criteria

Exclusion criteria for Cervical Spondylotic Myelopathy patients:

1. Patients who underwent decompression surgery for more than once

2. Patients with Cervical Myelopathy due to traumatic etiology

3. Patients having history of any musculoskeletal injuries or disability, peripheral nerve injury of

lower limb, that may interfere with standing ability.

4. Patients not willing to participate

Exclusion criteria for aged and gender matched normative participants:

1. Participants having history of any musculoskeletal injuries or disability, peripheral nerve injury

of lower limb, that may interfere with standing ability

2. Participants not willing to participate

3. Participants with diabetic neuropathy

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Amcube Foot work pro- electronic pedometer <br/ ><br>2. Lower Extremity Functional Scale (LEFS) <br/ ><br>3. Falls Efficacy Scale- International (FES-I) <br/ ><br>4. Visual Analogue scale (VAS)35Timepoint: Baseline

Secondary Outcome Measures

Name	Time	Method
nilTimepoint: nil