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Morning or night rehab? new study tests best time for back pain Patients' sleep

NCT ID NCT07522021

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether doing physical therapy in the daytime or evening helps people with a herniated disc in their lower back sleep better and feel less sleepy during the day. It includes 60 adults who also have a high risk for obstructive sleep apnea. Participants will be randomly assigned to a daytime or evening rehab program, and their sleep quality, daytime sleepiness, pain, and function will be measured.

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

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Nov 2026

An estimate. End dates often move.

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 65 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: * Individuals aged 18-65 years * High risk for obstructive sleep apnea, defined as a score \>4 on the STOP-Bang questionnaire (Snoring, Tiredness, Observed apnea, high blood pressure, Body mass index, Age, Neck circumference, and Gender) * Presence of lumbar disc herniation (bulging, protrusion, or extrusion) at L1-S1 levels confirmed by magnetic resonance imaging (MRI) * Chronic low back pain lasting at least 3 months with clinical symptoms consistent with imaging findings * Mild to moderate radicular symptoms For participants over 55 years of age: single-level or dominant-level protrusion or extrusion-type disc herniation to minimize confounding effects of multilevel degeneration * Pain intensity ≥4 on the Visual Analog Scale (VAS) within the last week * Ability to participate regularly in the physiotherapy and rehabilitation program * Willingness to provide written informed consent Exclusion Criteria: * Presence of sequestrated disc herniation or cauda equina compression confirmed by magnetic resonance imaging (MRI) * Progressive motor deficit or significant muscle weakness * Indication for urgent surgical intervention * History of previous lumbar spine surgery * Low back pain due to specific causes (e.g., spinal tumor, infection such as spondylodiscitis, inflammatory rheumatic diseases, or traumatic fracture) * Previous use of continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) therapy * Shift work or irregular sleep patterns * Major changes in sleep medication within the last 4 weeks * Contraindications to electrotherapy (e.g., pacemaker or implanted electronic devices, suspected malignancy, sensory loss in the treatment area, open wounds, or infection) * Cardiopulmonary conditions that contraindicate exercise * Uncontrolled hypertension or advanced heart failure * Pregnancy * Severe psychiatric disorders or cognitive impairment * Neurological disorders (e.g., multiple sclerosis, stroke sequelae) * Epidural or facet joint injection within the last 3 months * Diagnosed severe obesity hypoventilation syndrome or severe chronic obstructive pulmonary disease (COPD) * Refusal to provide informed consent

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Conditions

The condition(s) this trial relates to.

Disorders of Excessive Somnolence insomnia Intervertebral Disc Displacement lumbar disk disease lumbar disk herniation, susceptibility to

As listed by the trial registrant

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

How to take part

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  1. The official record

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