Lumbar Disc DegenerationNCT07547410
Application of Internet Plus Nursing Intervention in Postoperative Rehabilitation of Patients With Lumbar Disc Herniation
A study testing Internet plus applet in people with Lumbar Disc Degeneration, run by The Fourth Affiliated Hospital of Zhejiang University School of Medicine at 1 site in China.
Trial summary
The purpose of this observational study is to understand the influence of rehabilitation guidance through Internet plus mini program on the compliance of patients at home rehabilitation exercise who have undergone lumbar discectomy at the age of 18-59 years. Read more about this study
- Who is it for?
- Ages 18 to 59 years
- Conditions the study is for
- Lumbar Disc Degeneration
- What is being tested?
- Internet plus applet
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteChina
- Study dates
- 20 Feb 2024to 10 Nov 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 59 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Diagnosed as LDH through physical examination and imaging examination;
- It is planned to undergo lumbar discectomy surgery at the Fourth Affiliated Hospital of Zhejiang University School of Medicine;
- Age range of 18 to 59 years old;
- Clear consciousness and communication skills Good strength and reading ability.
Who cannot join
- Non discogenic lower back and leg pain;
- There are serious diseases of other organs, or other serious complications, or inability to take care of oneself;
- Past or current mental illness, severe cognitive impairment, or communication barriers;
- Due to other reasons, I withdrew midway and cannot continue to participate in this study.
Trial locations and contacts
1 site in 1 country.
China1 site
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Yiwu, Zhejiang, 322000
About this study
The purpose of this observational study is to understand the influence of rehabilitation guidance through Internet plus mini program on the compliance of patients at home rehabilitation exercise who have undergone lumbar discectomy at the age of 18-59 years. The main question it wants to answer is:
Can rehabilitation guidance for patients after lumbar discectomy through Internet plus applet effectively improve the compliance of patients with home rehabilitation exercise? Participants receiving rehabilitation guidance via Internet plus applet after routine intervention measures need to answer online questionnaire questions about compliance of home rehabilitation exercise for 6 months.
- Conditions
- Lumbar Disc Degeneration
- Being tested
- Internet plus applet
- Medical subject headings
- Intervertebral Disc Degeneration
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Internet plus appletBehavioural
- At 8am and 2pm every day, push notification messages to remind patients to engage in functional exercises;
- Rehabilitation exercise videos: including methods, steps, and exercise precautions for various functional exercises;
- Vividly present the daily life precautions after lumbar disc herniation surgery through various means such as graphics, videos, etc;
- Doctor patient interaction, setting up a liaison nurse every day to answer questions raised by patients;
- Sharing section, where professionals form groups based on patients' disease experiences, cultural backgrounds, and other information to promote mutual communication and learning among patients with lumbar disc herniation through this sharing platform;
- Check in function (including graphics, images, and videos), where professionals can choose a suitable rehabilitation exercise plan based on the patient's recovery situation, dynamically evaluate the patient's needs, and promote their recovery;
- Smart questionnaire
| Study group | Role | What they receive |
|---|---|---|
| control group | No intervention | Not described |
| intervention group | Active comparator | internet plus applet Receives: Behavioral: Internet plus applet |
What is being measured
The primary outcome is the main question the study is designed to answer.
score on the compliance behavior scale for postoperative patients with lumbar intervertebral disc herniation
Patient Compliance Behavior Scale The highest score is 100 points Minimum score 0 The higher the score, the better the patient's adherence to medical treatment
Measured: ６months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Apr 2026
- Study start20 Feb 2024
- Primary completion10 Nov 2024
- Study completion10 Nov 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Lumbar Disc DegenerationStudies of the same condition, open and under way.
- More trials run by The Fourth Affiliated Hospital of Zhejiang University School of MedicineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07547410
- Sponsor's protocol ID
- KY-2023-190
- Status last verified
- Mar 2026
- First submitted
- 30 Mar 2026
- Last updated
- 23 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Publications
Ruan Y, Zheng D, Chu W, Yu J. The application effect of mobile internet technology in the postoperative follow-up management of patients with lumbar intervertebral disc protrusion. Front Surg. 2026 Aug 31;13:1876447. doi: 10.3389/fsurg.2026.1876447. eCollection 2026.
PubMed 42741418
Study at a glance
From the registry record, last updated by the sponsor on 23 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Application of Internet Plus Nursing Intervention in Postoperative Rehabilitation of Patients With Lumbar Disc Herniation
- ClinicalTrials.gov ID
- NCT07547410
- Acronym / sponsor ID
- KY-2023-190
- Conditions
- Lumbar Disc Degeneration
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- The Fourth Affiliated Hospital of Zhejiang University School of MedicineUniversity, hospital or other
- Study start
- 20 Feb 2024 (actual)
- Primary completion
- 10 Nov 2024 (actual)
- Study completion
- 10 Nov 2024 (actual)
- First posted
- 23 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this observational study is to understand the influence of rehabilitation guidance through Internet plus mini program on the compliance of patients at home rehabilitation exercise who have undergone lumbar discectomy at the age of 18-59 years. The main question it wants to answer is:
Can rehabilitation guidance for patients after lumbar discectomy through Internet plus applet effectively improve the compliance of patients with home rehabilitation exercise? Participants receiving rehabilitation guidance via Internet plus applet after routine intervention measures need to answer online questionnaire questions about compliance of home rehabilitation exercise for 6 months.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| control group | No intervention | – |
| intervention group | Active comparator | Behavioral: Internet plus appletinternet plus applet |
Who may qualify
- Ages
- 18 to 59 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- Diagnosed as LDH through physical examination and imaging examination;
- It is planned to undergo lumbar discectomy surgery at the Fourth Affiliated Hospital of Zhejiang University School of Medicine;
- Age range of 18 to 59 years old;
- Clear consciousness and communication skills Good strength and reading ability.
Key exclusion criteria (4 listed)
- Non discogenic lower back and leg pain;
- There are serious diseases of other organs, or other serious complications, or inability to take care of oneself;
- Past or current mental illness, severe cognitive impairment, or communication barriers;
- Due to other reasons, I withdrew midway and cannot continue to participate in this study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Internet plus applet1. At 8am and 2pm every day, push notification messages to remind patients to engage in functional exercises; 2. Rehabilitation exercise videos: including methods, steps, and exercise precautions for various functional exercises; 3. Vividly present the daily life precautions after lumbar disc herniation surgery through various means such as graphics, videos, etc; 4. Doctor patient interaction, setting up a liaison nurse every day to answer questions raised by patients; 5. Sharing section, where professionals form groups based on patients' disease experiences, cultural backgrounds, and other information to promote mutual communication and learning among patients with lumbar disc herniation through this sharing platform; 6. Check in function (including graphics, images, and videos), where professionals can choose a suitable rehabilitation exercise plan based on the patient's recovery situation, dynamically evaluate the patient's needs, and promote their recovery; 7. Smart questionnaire | Behavioural | intervention group |
Primary outcome
score on the compliance behavior scale for postoperative patients with lumbar intervertebral disc herniation
Time frame: ６months
Patient Compliance Behavior Scale The highest score is 100 points Minimum score 0 The higher the score, the better the patient's adherence to medical treatment
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Apr 2026.
- Derived from this study: PubMed 42741418Ruan Y, Zheng D, Chu W, Yu J. The application effect of mobile internet technology in the postoperative follow-up management of patients with lumbar intervertebral disc protrusion. Front Surg. 2026 Aug 31;13:1876447. doi: 10.3389/fsurg.2026.1876447. eCollection 2026.
- Individual participant dataSharing planned: Yes
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Internet plus applet in people with Lumbar Disc Degeneration, run by The Fourth Affiliated Hospital of Zhejiang University School of Medicine at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 23 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
score on the compliance behavior scale for postoperative patients with lumbar intervertebral disc herniation (time frame: ６months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07547410, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Apr 2026.