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Could fear of movement slow spine surgery recovery?

NCT ID NCT07762183

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time

Summary

This study looks at whether a patient's frailty, dependence in daily activities, and fear of movement before surgery affect how well they move and care for themselves right after lumbar disc herniation surgery. Researchers will assess these factors before surgery and on the first day after surgery in about 221 adults. The goal is to identify risk factors that could help nurses create more personalized care and rehabilitation plans.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If certain pre-surgery factors are linked to slower recovery, this could help nurses personalize care plans to improve early mobilization and self-care after spine surgery.
What could go wrong
This is an observational study, so it can only show connections, not cause and effect. The results may not apply to all spine surgery patients or other hospitals.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

221 people

The number who actually took part.

Started

Dec 2025

Finished

Jun 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults (≥18 years) undergoing elective lumbar disc herniation surgery in the Neurosurgery Clinic of Aydın Adnan Menderes University Research and Application Hospital who meet the eligibility criteria and provide informed consent will be consecutively enrolled in the study.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Aged 18 years or older * Able to speak and understand Turkish * Having no hearing impairment that would prevent communication * Scheduled to undergo lumbar disc herniation surgery * Conscious and clinically able to complete the preoperative assessments * Conscious and clinically stable on postoperative day 1 to allow assessment of mobilization and self-care agency * Voluntarily agreeing to participate in the study and providing informed consent Exclusion Criteria: * Having a diagnosed psychiatric disorder documented in the medical record or reported by the clinical team * Being unable to complete the data collection forms because of cognitive, communication, or clinical limitations * Developing a postoperative condition that prevents mobilization or self-care assessment on postoperative day 1 * Withdrawing consent at any stage of the study

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Aydın Adnan Menderes University

    Aydin, Zafer Mahallesi, 09010, Turkey (Türkiye)

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