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Application of Internet Plus Nursing Intervention in Postoperative Rehabilitation of Patients With Lumbar Disc Herniation

NCT07547410 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-04-23

No results posted yet for this study

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. 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

Interventions

BEHAVIORAL

Internet plus applet

1. 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

Sponsors & Collaborators

  • The Fourth Affiliated Hospital of Zhejiang University School of Medicine

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
59 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-20
Primary Completion
2024-11-10
Completion
2024-11-10

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07547410 on ClinicalTrials.gov