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NCT04927507 Clinical Trial

Rotator Cuff Injury Managed With ERAS and Internet Plus Nursing

Rotator Cuff Injuries Clinical Trial

Official title:
Rotator Cuff Injury Managed With ERAS and Internet Plus Nursing

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04927507
Other study ID # 2021-0061
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2022

Study information
Verified date June 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Ping Qian
Phone 0571-87783777
Email 13208118@qq.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Rotator cuff injury patients treated with ERAS were included. The control group was given routine nursing. The observation group was given the Internet plus nursing home rehabilitation mode. Relying on mobile app and wechat, patients can get online guidance of rehabilitation training video through app and wechat, and get professional rehabilitation guidance at any time.

Recruitment information / eligibility
Status Recruiting
Enrollment 140
Est. completion date December 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Rotator cuff injury - ERAS surgery treatment - Full thickness tear of rotator cuff, The range of tear is 1cm-3cm Exclusion Criteria: - Surgery not applicable - Combined with other injuries, malignant tumor, disabilities, mental illness, critically ill patients, pregnant women, illiteracy, minors, cognitive impairment

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Internet plus nursing home rehabilitation
The observation group was given the Internet plus nursing home rehabilitation mode. Relying on mobile app and wechat public service platform, patients can get online guidance of rehabilitation training video through app and wechat, and get professional rehabilitation guidance at any time.

Locations
Country Name City State
China Ping Qian Hangzhou

Sponsors (1)
Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary The Constant-Murley score The Constant-Murley score (CMS) is a 100-points scale composed of a number of individual parameters. These parameters define the level of pain and the ability to carry out the normal daily activities of the patient. The Constant-Murley score was introduced to determine the functionality after the treatment of a shoulder injury. The best situation is 100 points. The worst situation is 0 points. up to 6 months
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