Investigation of the effectiveness of a Telerehabilitation-Based exercise program after lumbar disc herniation surgery
NCT ID NCT07889817
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.
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
-
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 Hide 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
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Lumbar disc herniation are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
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)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can standing up sooner speed recovery after back surgery?
- Face-Down surgery: does breathing mechanics affect brain oxygen?
- Ozone gas injected into slipped discs: a new way to stop leg pain?
- Can a taller fluid bag make spine surgery safer?
- Can contrast spread predict which sciatica injection works?
- Back therapy may give lungs a boost: trial tests breathing benefits