Assessment and Rehabilitation in Cervical Radiculopathy

NAEnrolling by invitationINTERVENTIONAL
Enrollment

110

Participants

Timeline

Start Date

May 10, 2025

Primary Completion Date

May 14, 2025

Study Completion Date

August 15, 2025

Conditions
Cervical Radicular PainSpondyloarthritis (SA)Neuropathic Pain ManagementQuality of Life (QOL)
Interventions
COMBINATION_PRODUCT

All patients in the study will be included in rehabilitation program

A total of 110 consecutive participants with previous diagnosed CR lasting more than 3 months will be enrolled in this study. After initial assessment, participants without surgical recommendation, will be included into two groups: Study Group will be received 10 sessions of rehabilitation program and nutraceutical product daily, 3 months, and Control Group will be received 10 sessions of rehabilitation program. The rehabilitation program include physical therapy (electrical muscle stimulation of the neck muscle and upper limb muscles , low-Level Laser Therapy and ultrasound) and kinetic training.

DIETARY_SUPPLEMENT

Study Group will receive a nutraceutical product daily, 3 months.

Study Group will receive a nutraceutical product daily, 3 months in addition to the rehabilitation program.

Trial Locations (1)

1100

Diana Kamal, Craiova

All Listed Sponsors
lead

Filantropia Hospital

OTHER