Pain Monitoring of Herniated Disc Surgery Patients With Oura Ring

Status Recruiting

Clinical Trial Summary

The objective of this research study is to show whether data given by Oura ring could be used to objectively measure patients pain and well-being before and after disc surgery.

Clinical Trial Description

The study will consist of a total 30 disc prolapse patients. Patients are given Oura rings along with other treatment. Patients use Oura rings before and after disc surgery. Patients will also fill Beck Depression Inventory (BDI) and pain detect inquiries in the beginning and in the end of study. Patients symptoms will also be followed daily by electrical symptom diary. Oura rings technology is based on photoplethysmography( PPG). PPG is a noninvasive method to detect blood volume changes in the microvascular bed of tissue. PPG waveform varies by respiration, sympathetic nervous system activity and thermoregulation. Oura ring gives information of patients activity level, calorie consumption, steps count, resting heart rate,heart rate variability, respiration rate, body temperature, sleep depth and quality of sleep. Data collected with Oura ring after disc surgery will be compared to data collected before surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05129007
Study type	Observational
Source	Tampere University Hospital
Contact	Tommi Bergman, Md
Phone	0331166356
Email	tommi.bergman@pshp.fi
Status	Recruiting
Phase
Start date	November 1, 2022
Completion date	December 31, 2024

View Details

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