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Synchronous and Asynchronous Telerehabilitation Methods in Patients With Shoulder Tendinopathy

M

Marmara University

Status

Enrolling

Conditions

Shoulder Pain
Tendinopathy

Treatments

Other: Asynchronous Exercise Program
Other: Synchronous Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT05549817
2022/67

Details and patient eligibility

About

This study is a randomized controlled trial conducted to compare the effects of synchronous and asynchronous telerehabilitation programs on pain, disability, and quality of life parameters in patients with shoulder tendinopathy in the Marmara University Physiotherapy and Rehabilitation Department.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants between the ages of 18-65,
  • Who had access to the internet and smartphone,
  • Had the ability to conduct video calls included in the study.

Exclusion criteria

  • Participants were excluded if they had COVID-19,
  • Had surgery in the last 6 months,
  • Had neurological and psychological disorders,
  • Received physiotherapy treatment.
  • Had surgery in the last 6 months,
  • Had a condition that prevented them from exercising.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Synchronous Telerehabilitation Group
Experimental group
Description:
The exercise program was applied to groups that include three participants of the synchronous group 3 days per week by video conference method on an online platform (Zoom) with the supervision of a physiotherapist. The time of the group session was organized according to the availability of participants in that group and the physiotherapist using shared calendar availability (Doodle). The physiotherapist sent a reminder to participants one hour prior to each session including the video conference meeting link. Each exercise session lasted approximately 40 minutes. For 8 weeks, a total of 24 exercise sessions were performed. The physiotherapist demonstrated the exercises as needed, supervised the group by giving real-time feedback, and progressed the exercise program according to the needs of each group.
Treatment:
Other: Synchronous Exercise Program
Asynchronous Telerehabilitation Group
Active Comparator group
Description:
The exercise program was prescribed and followed up 3 days per week via the mobile application (FizyoTr). A notification was sent to participants' phones via mobile application prior to each session and attendance to the exercise program was recorded. For 8 weeks, a total of 24 exercise sessions were performed. The physiotherapist progressed the exercise program according to the assessment at 4 weeks and the needs of each participant.
Treatment:
Other: Asynchronous Exercise Program

Trial contacts and locations

1

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Central trial contact

Eren Timurtaş, Ph.D.

Data sourced from clinicaltrials.gov

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