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

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 Overview

• Status: Completed
• Conditions: Lumbar Disc Degeneration
• Intervention / Treatment: Behavioral: Internet plus applet

• Study Type: Interventional
• Enrollment (Actual): 100
• Phase: Not Applicable

Contacts and Locations

Study Locations

• China
  • Zhejiang
    • Yiwu, Zhejiang, China, 322000
      • The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• 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.

Exclusion Criteria:

• 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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
No Intervention: control group
Active Comparator: intervention group; internet plus applet	Behavioral: Internet plus applet; 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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	６months

Collaborators and Investigators

• Sponsor: The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Study record dates

Study Major Dates

• Study Start (Actual): February 20, 2024
• Primary Completion (Actual): November 10, 2024
• Study Completion (Actual): November 10, 2024

Study Registration Dates

• First Submitted: March 30, 2026
• First Submitted That Met QC Criteria: April 16, 2026
• First Posted (Actual): April 23, 2026

Study Record Updates

• Last Update Posted (Actual): April 23, 2026
• Last Update Submitted That Met QC Criteria: April 16, 2026
• Last Verified: March 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Bone Diseases; Musculoskeletal Diseases; Spinal Diseases; Intervertebral Disc Degeneration
• Other Study ID Numbers: KY-2023-190

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Sharing Supporting Information Type: ICF

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No