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Pain Monitoring of Herniated Disc Surgery Patients With Oura Ring

Pain Monitoring of Herniated Disc Surgery Patients With Oura Ring

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05129007
Enrollment
30
Registered
2021-11-22
Start date
2022-11-01
Completion date
2024-12-31
Last updated
2023-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Measurement

Keywords

Pain, Oura ring, Activity measurment, Herniated disc

Brief 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.

Detailed 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.

Interventions

DEVICEOura ring

Photopletysmography based noninvasive device

Sponsors

Oura health oy
CollaboratorUNKNOWN
Tampere University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Upcoming herniated disc surgery, ability to give a written informed concent

Exclusion criteria

* Sleep apnea, Condition with irregular heart rate, lack of cooperation

Design outcomes

Primary

MeasureTime frameDescription
Change in symptoms based on symptom diaryprior surgery and one month after surgeryDaily symptom diary kept by patient
Change in total sleep timecomparison of mean value prior to surgery and one month after surgerycollected from oura ring
Change in sleep stages (awake, light sleep, deep sleep and rem sleep)comparison of mean value prior to surgery and one month after surgerypercentages of each sleep stages collected from oura ring
Change in heart rate variabilitycomparison of mean value prior to surgery and one month after surgerycollected from Oura ring
Change in resting mean heart ratecomparison of mean value prior to surgery and one month after surgerycollected from Oura ring
Change in ventilatory ratecomparison of mean value prior to surgery and one month after surgerycollected from oura ring
Change in sleep onset latencycomparison of mean value prior to surgery and one month after surgerycollected from oura ring
Change in sleep efficiencycomparison of mean value prior to surgery and one month after surgerypercentage of the time spent asleep while in bed collected from oura ring
Change in number of nighttime awakeningscomparison of mean value prior to surgery and one month after surgerycollected from oura ring

Secondary

MeasureTime frameDescription
Change in pain questionnaireone month prior surgery and one month after surgeryDescriptive questionnaire
Change in BDI questionnaire pointsone month prior surgery and one month after surgeryBECK Depression Inventory (Scale 1-63, higher scores mean a worse outcome)

Countries

Finland

Contacts

Primary ContactTommi Bergman, Md
tommi.bergman@pshp.fi0331166356
Backup ContactJarkko Harju, md, phd
jarkko.harju@fimnet.fi

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026