- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06828133
Egyptian Physical Therapists' Perceptions of Tele- Rehabilitation
February 10, 2025 updated by: Ebtihal Abdelaal Eissa Ali, Cairo University
Egyptian Physical Therapists' Perceptions of Tele- Rehabilitation: an Online Open Survey on Acceptability, Preferences, and Needs
The healthcare industry has undergone a significant transformation with the integration of digital technologies, and one of the notable advancements in this field is tele-rehabilitation.
Tele-rehabilitation, a subset of telehealth, involves the use of digital platforms to deliver physical therapy services remotely.
This innovative approach allows healthcare providers to extend their reach, offering therapy to patients who might otherwise face barriers to accessing care,tele-rehabilitation has been recognized for its numerous benefits.
It enhances access to physical therapy services, particularly for individuals living in remote or underserved areas.
By reducing the need for travel, tele-rehabilitation offers significant convenience to patients, enabling them to receive therapy in the comfort of their homes.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
2000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: ebtihal abdelaal eissa
- Phone Number: 01140088171
- Email: ebtihalabdelall@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
both male and female age between equale and more 25
Description
- Must be a licensed physical therapist with at least 3 years of experience practicing in Egypt.
- Must be 25 years of age or older.
- Must have access to the internet and be able to complete an online survey.
- Available to complete all survey-related questions.
Exclusion Criteria:
- Not currently practicing as a physical therapist.
- Diagnosed with conditions that impair the ability to complete an online survey.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
observithional study of this group
observitional of this study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
acceptability
Time Frame: 6 months
|
questionnaire
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
preferences
Time Frame: 6 month
|
quthionnaire
|
6 month
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
needs
Time Frame: 6 mnoth
|
quthionnaire
|
6 mnoth
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
April 1, 2025
Primary Completion (Estimated)
October 1, 2025
Study Completion (Estimated)
November 1, 2025
Study Registration Dates
First Submitted
February 10, 2025
First Submitted That Met QC Criteria
February 10, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 10, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- P.T.REC/012/005612
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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