Morning or night rehab? new study tests best time for back pain Patients' sleep
NCT ID NCT07522021
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.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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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.
As listed by the trial registrant
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How to take part
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The official record
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