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Smartphone app may cut complications after disc surgery

NCT ID NCT06770387

Symptom relief Sponsor: Hasan Kalyoncu University Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested whether a mobile app and telenursing follow-up could improve recovery after lumbar disc surgery. 107 patients were enrolled. The approach aimed to reduce falls, anxiety, and complications after discharge.

What this could mean

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

Active substance
mobile application for postoperative care
What this could lead to
If it works, this could point toward a better way to support recovery after back surgery, reducing complications and anxiety.
What could go wrong
This is a small, completed study without a treatment drug. Results may not apply to all patients or settings.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

107 people

The number who actually took part.

Started

Dec 2024

Finished

May 2025

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.

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: * Patients who are 18 years of age or older, * Can speak and understand Turkish, * Have no hearing, understanding, vision or speech problems, * Have undergone LDH surgery for the first time, * Have undergone LDH surgery with the open method, * Have not been diagnosed with depression or anxiety disorder before surgery and are not taking medication for this purpose, * Have a smart mobile phone suitable for taking photos or for those close to them, * Have not developed serious complications that would delay their discharge from the hospital, * Volunteer to participate in the study will be included in the study. Exclusion Criteria: * Patients who wish to withdraw from the study at any stage after voluntarily participating in the study.

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Conditions

The condition(s) this trial relates to.

lumbar disk herniation, susceptibility to

As listed by the trial registrant

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

Lumbar disc surgery

Contacts and locations

Locations

  • Deva Hospital

    Gaziantep, 27027, Turkey (Türkiye)

  • Gaziantep University Şahinbey Research and Application Hospital

    Gaziantep, 27027, Turkey (Türkiye)

  • Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital

    Kahramanmaraş, 46046, Turkey (Türkiye)

  • Medical Point Hospital

    Gaziantep, 27027, Turkey (Türkiye)

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