NCT03961802

Early and Systematic Shoulder Rehabilitation Following Cervical Lymph Node Dissection

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 120 (actual)
• Sponsor: Nantes University Hospital · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

A prospective, monocentric, controlled, randomized study of systematic early shoulder rehabilitation following cervical lymph node dissection for the prevention and treatment of shoulder dysfunction.

Detailed description

Pre-inclusion: information, collection of consent, collection of antecedents and biometric data, clinical examination (goniometric measurement and visual analogic scale of pain), collection of DASH, EORTC QLQ-C30 and H\&N35 questionnaires. Surgical intervention (J0) and randomization into 2 groups: Group 1 - systematic early rehabilitation Group 2 - without systematic rehabilitation M3, M6, M12: collection of complications, adjuvant treatments, number of physiotherapy sessions performed, clinical examination (goniometric measurement and visual analogic scale of pain), collection of DASH, EORTC QLQ- C30 and H\&N35 questionnaires.

Conditions

• Rehabilitation

Interventions

Type	Name	Description
OTHER	sessions of shoulder rehabilitation	3 sessions of shoulder rehabilitation per week for 3 months (36 sessions)

Timeline

• Start date: 2019-07-02
• Primary completion: 2023-11-16
• Completion: 2023-11-16
• First posted: 2019-05-23
• Last updated: 2024-01-24

Locations

1 site across 1 country: France