Investigation of the effectiveness of a Telerehabilitation-Based exercise program after lumbar disc herniation surgery

NCT ID NCT07889817

What the study statuses mean

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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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Oct 22, 2026 · Last updated Oct 22, 2026

Summary

This randomized controlled trial evaluated the effectiveness of a telerehabilitation-based exercise program in individuals who had undergone surgery for lumbar disc herniation. Participants were assigned to a control group, a home exercise group, or a telerehabilitation group. The exercise programs started four weeks after surgery and continued for eight weeks, three days per week, with each session lasting 30-45 minutes. The home exercise group performed the exercise program independently at home, while the telerehabilitation group performed the same program under remote supervision of a physiotherapist using video calls. The control group continued their routine daily activities without participating in a structured exercise program during the study period. Pain, disability, physical activity, and health-related quality of life were assessed before and after the eight-week intervention period.

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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

82 people

The number who actually took part.

Started

Dec 2024

Finished

Oct 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.

Ages

18 to 60 years

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: * Participants who had undergone lumbar disc herniation surgery four weeks previously * Age between 18 and 60 years * Voluntary agreement to participate in the study Exclusion Criteria: * Presence of cognitive or physical health problems that could prevent participation in the study * Use of analgesic or muscle relaxant medication

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Conditions

The condition(s) this trial relates to.

Intervertebral Disc Displacement lumbar disk disease Motor Activity Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Inonu University Turgut Ozal Medical Center

    Malatya, 44280, Turkey (Türkiye)

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