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Spots Global Cancer Trial Database for Early and Systematic Shoulder Rehabilitation Following Cervical Lymph Node Dissection

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Trial Identification

Brief Title: Early and Systematic Shoulder Rehabilitation Following Cervical Lymph Node Dissection

Official Title: Early and Systematic Shoulder Rehabilitation Following Cervical Lymph Node Dissection

Study ID: NCT03961802

Conditions

Rehabilitation

Study Description

Brief 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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Nantes University Hospital, Nantes, , France

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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