NCT06024551

Brief Summary

The goal of this study is to investigate the effect of telerehabilitation in patients with rotator cuff tendinopathy. The main questions it aims to answer are:

  • Is telerehabilitation effective in improving the functional status of patients with rotator cuff tendinopathy?
  • Is telerehabilitation effective in reducing the pain of rotator cuff patients?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
34

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 4, 2023

Completed
5 months until next milestone

First Posted

Study publicly available on registry

September 6, 2023

Completed
3 months until next milestone

Study Start

First participant enrolled

December 15, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2024

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2024

Completed
Last Updated

August 9, 2024

Status Verified

August 1, 2024

Enrollment Period

1 month

First QC Date

April 4, 2023

Last Update Submit

August 8, 2024

Conditions

Keywords

rotator cuff tendinopathytelerehabilitation

Outcome Measures

Primary Outcomes (2)

  • Western Ontario Rotator Cuff Index

    Western Ontario Rotator Cuff Index is a disease-specific quality of life questionnaire, evaluating the change in symptoms and functional ability, specific to a Rotator Cuff tendinopathy. Raw scores range from 0 to 2100 with a higher score indicating decreased quality of life.

    one month

  • Simple Shoulder Test

    A questionnaire about the function of the involved shoulder. Overall scored is calculated by number of yes/number of completed items. Minimum score is 0 %and maximum is 100 %. Higher scores indicate better function.

    one month

Secondary Outcomes (1)

  • Range of motion

    one month

Study Arms (2)

Intervention Group

EXPERIMENTAL

Patients who receive telerehabilitation

Other: Telerehabilitation

Control Group

OTHER

Patients who receive home exercise program

Other: home exercise program

Interventions

Patients in this arm will be given telerehabilitation three times a week, for four weeks.

Intervention Group

Patients in this arm will receive home exercise program for four weeks

Control Group

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Diagnosis of Rotator cuff tendinopathy
  • Being able to do the prescribed exercises
  • Having an access to internet and having a computer or smart phone for telerehabilitation

You may not qualify if:

  • Patients with a neurological disease that may affect the effectiveness of exercise
  • History of fracture in shoulder region
  • History of surgery in shoulder region
  • Patients with a psychiatric disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Izmir Democracy University

Izmir, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Rotator Cuff Injuries

Interventions

Telerehabilitation

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon Injuries

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and ServicesTelemedicineDelivery of Health CarePatient Care ManagementHealth Services Administration

Study Officials

  • Ferruh Taşpınar

    Izmir Democracy University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

April 4, 2023

First Posted

September 6, 2023

Study Start

December 15, 2023

Primary Completion

January 15, 2024

Study Completion

June 15, 2024

Last Updated

August 9, 2024

Record last verified: 2024-08

Locations