Tele-rehabilitation in Patients Operated for Distal Radius Fracture
NCT ID: NCT05537493
Last Updated: 2023-05-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
46 participants
INTERVENTIONAL
2022-05-25
2023-05-11
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effectiveness of Instrument-Assısted Soft Tissue Mobılızatıon in Patients With Operated Distal Radius Fracture
NCT06194604
Mobilization With Movement in Distal Radial Fractures
NCT05976724
The Effect of Motor Imagery in Patients With Radius Distal End Fracture
NCT05360836
Are Rehabilitation Results in Flexor Tendon Zone II Injuries as Bad as Feared?
NCT06112145
Sensory Training in Distal Radius Fractures
NCT06894485
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Telerehabilitation
Videos of the exercises they will do via whatsapp will be sent to the telerehabilitation group. Again, in telerehabilitation, whatapp application will be made in the form of videoconference. Rehabilitation program will be applied to the patients 4 times a week for 6 weeks.
Telerehabilitation
It will be followed by exercising on whatsapp
Face to face
A rehabilitation program will be applied to the Face to Face rehabilitation group by a physiotherapist in the hospital for a total of 30 sessions per week for 6 weeks.
Face to face
It will be followed by face to face
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Telerehabilitation
It will be followed by exercising on whatsapp
Face to face
It will be followed by face to face
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients not having undergone any surgery on that extremity before, not having an extremity defect that prevents rehabilitation
* Patients with normal pre-fracture cognitive functions
* Patients without major postoperative complications
Exclusion Criteria
* Previous extremity-related surgery
* Injury in more than one anatomical region in the relevant extremity
* Patients living alone at home
* Malignancy, presence of known rheumatological disease, pregnancy
* Patients receiving any treatment other than the planned treatment
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ahi Evran University Education and Research Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Levent Horoz
Assist Prof
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Levent Horoz, Asisst Prof
Role: PRINCIPAL_INVESTIGATOR
Kirsehir Ahi Evran Universitesi
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ahi Evran University
Kirşehir, City Centre, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Bini SA, Mahajan J. Clinical outcomes of remote asynchronous telerehabilitation are equivalent to traditional therapy following total knee arthroplasty: A randomized control study. J Telemed Telecare. 2017 Feb;23(2):239-247. doi: 10.1177/1357633X16634518. Epub 2016 Jul 9.
Kane LT, Thakar O, Jamgochian G, Lazarus MD, Abboud JA, Namdari S, Horneff JG. The role of telehealth as a platform for postoperative visits following rotator cuff repair: a prospective, randomized controlled trial. J Shoulder Elbow Surg. 2020 Apr;29(4):775-783. doi: 10.1016/j.jse.2019.12.004.
Pastora-Bernal JM, Martin-Valero R, Baron-Lopez FJ, Moyano NG, Estebanez-Perez MJ. Telerehabilitation after arthroscopic subacromial decompression is effective and not inferior to standard practice: Preliminary results. J Telemed Telecare. 2018 Jul;24(6):428-433. doi: 10.1177/1357633X17706583. Epub 2017 Apr 27.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KAEK_2022-09/96
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.