An interventional study of post-discharge rehabilitation training in Spine Disease and Spinal Deformity, sponsored by Çanakkale Onsekiz Mart University. Recruiting at 1 site in Turkey. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-01-05.
Sponsored by Çanakkale Onsekiz Mart University · Not applicable, Interventional, and Supportive care
The aim is to quantify the fear of movement and quality of life of telephone education on lumbar disc herniation surgery.
In the randomized controlled study, patients will be randomized into two categories: experimental and control groups. The experimental group will receive intervention via online information for 6 weeks after discharge. The control group will not be given online training other than standard nursing care. At the end of 6 weeks, the difference between fear of movement and quality of life between the two groups will be examined.
174 studies on the registry are indexed under Spinal Diseases; 39 are open to participants now.
This study's planned enrollment of 80 is above the median of 60 across 106 interventional studies indexed under Spinal Diseases.
Browse Spinal Diseases studies →Çanakkale Onsekiz Mart University is the lead sponsor of 51 studies on the registry; 15 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
This group will be trained by phone for 6 weeks after discharge.
Behavioral: post-discharge rehabilitation training
This group will be given training during their stay in the hospital. There will be no training over the phone after discharge.
Telephone training will be provided for post-discharge rehabilitation
Also known as: nursingcare, nursing education
movement fear scale
In the measurement to be made with a four-point Likert type scale, 17 is the lowest score and 68 is the highest score. The higher the score the patient receives, the greater the fear of movement.
Time frame: six week
quality of life scale
The score obtained from the scale varies between 0 and 100. As the score obtained from the scale increases, the patient's quality of life increases.
Time frame: six week
Plan to share: No
No publications or documents are linked to this record.
Started Dec 2023 (actual). Primary completion is estimated for Jan 2025, 13 months after the start.
Of 40 non-industry interventional studies with no phase under Spinal Diseases, half reached primary completion within 26 months of starting (the median), counting those still running; a quarter within 16 and three quarters within 50. This study's planned 13 months is below that.
Counting every sponsor, half of 43 studies reached it within 26 months; a quarter within 16 and three quarters within 60.
How these figures are worked out, and which studies are left out of them.
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
Contact study teamGet an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Çanakkale Onsekiz Mart University