Osteoporosis Clinical Trials

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Development and Application of a Clinical Decision Support System for Exercise Rehabilitation in Patients With Osteoporotic Vertebral Compression Fractures

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to develop a clinical decision support system for exercise rehabilitation in patients with osteoporotic vertebral compression fractures, based on evidence-based recommendations for postoperative exercise rehabilitation. The system is designed to provide individualized assessment and exercise interventions, monitor exercise behaviors, and deliver risk alerts, thereby promoting safe and standardized postoperative exercise training in OVCF patients. The ultimate objectives are to evaluate the feasibility and effectiveness of the system in increasing physical exercise participation, reducing sedentary time, and facilitating postoperative rehabilitation, without increasing fatigue or pain.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• age between 18 and 55 years

• diagnosis of lumbar disc herniation requiring single-level lumbar fusion surgery - no previous history of lumbar surgery

• Surgical procedures performed by the same surgical team

• willingness to comply with the study protocol and restrictions

• availability of a home WiFi connection

Locations
Other Locations
China
Affiliated 2 Hospital of Nantong University, Nantong, Jiangsu 0513
RECRUITING
Nantong
Contact Information
Primary
Hong GAO
2439220393@qq.com
13773643315
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2028-06-01
Participants
Target number of participants: 60
Treatments
Experimental: The intervention group
The experimental group received individualized assessment and exercise rehabilitation intervention through the clinical decision support system for exercise rehabilitation in patients with osteoporotic vertebral compression fractures.
Active_comparator: The control group
The control group received conventional postoperative care interventions
Related Therapeutic Areas
Sponsors
Leads: Jiawei Jiang

This content was sourced from clinicaltrials.gov