SPA: Smart Pain Assesment Tool Based on Internet of Things

Sponsor
University of Turku (Other)
Overall Status
Completed
CT.gov ID
NCT03061240
Collaborator
Academy of Finland (Other), Turku University Hospital (Other)
58
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Study Details

Study Description

Brief Summary

This study is the second phase of a research project called "Smart Pain Assessment Tool based on Internet-of-Things". During the course of this project, a smart pain assessment tool (SPA) to detect and assess pain employing behavioural and physiologic indicators will be developed. We aim to assess pain based on changes in electromyographic (EMG) activity in facial muscles, i.e. changes in facial expressions and simultaneously use physiologic signs such as heart rate, respiratory rate and galvanic skin response as adjuvant measures to develop an algorithm for pain assessment in critically ill patients.

Condition or Disease Intervention/Treatment Phase
  • Device: Smart pain assessment tool
N/A

Detailed Description

The aim of this "smart pain assessment tool based on internet of things" SPA-research project is to develop an automatic and versatile pain assessment tool algorithm for detection and assessment of pain in a reliable and objective way in non-communicative patients. The final objective of the research project is to develop a smart pain assessment tool to detect and assess pain employing behavioural and physiologic indicators for a wide range of users/patients from infants to elderly people who are unable to communicate normally. The research project consists of three clinical phases (European Commision. Meddev 2.7/4/2010). The clinical phase I of the research project focused on developing pain assessment techniques involuntary working-age healthy study subjects. This current Clinical phase II includes the further development and research of the smart pain assessment tool in elective (non emergency) postoperative surgical patients during their stay after surgery in a recovery room.

Study Design

Study Type:
Interventional
Actual Enrollment :
58 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Smart Pain Assesment Tool Based on Internet of Things
Actual Study Start Date :
Nov 20, 2017
Actual Primary Completion Date :
Jun 11, 2018
Actual Study Completion Date :
Jun 11, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Postoperative patients

We recruit postoperative patients who undergo open surgery and are not receiving local anesthesia. We install a smart pain assessment tool on patient's skin to capture different type of data.

Device: Smart pain assessment tool
We record and analyze multiple bio-signals from post-operative patients in the attempt to evaluate their experienced pain.

Outcome Measures

Primary Outcome Measures

  1. Facial muscle activity [2 hours after surgery when the subject has woken up]

    The device is designed for multi-channel EMG acquisition from facial skin. Measuring a combination of EMG signals and their energy level (amplitude).

Secondary Outcome Measures

  1. Skin conductance [2 hours after surgery when the subject has woken up]

    Galvanic skin response (GSR), also known as electrodermal activity (EDA) or skin conductance (SC).

  2. Pain assesment by VAS [2 hours after surgery when the subject has woken up]

    Subjective feeling of pain is asked every 10 minutes by using numeric visual analog scale (VAS), values are given from 0-10.

  3. Heart rate [2 hours after surgery when the subject has woken up]

    Heart rate is monitored and recorded.

  4. Respiratory rate [2 hours after surgery when the subject has woken up]

    Respiratory rate is monitored and recorded.

  5. Oxygen saturation [2 hours after surgery when the subject has woken up]

    Oxygen saturation is monitored and recorded.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subject is scheduled for major surgery that requires general anesthesia and is likely to cause moderate to severe pain postoperatively which needs to be treated with systemic analgesics

  • Ability to communicate

  • Written informed consent

  • Healthy facial skin

Exclusion Criteria:
  • Subject treated with local anesthesia during surgery

  • Any diagnosed condition affecting cognitive functions

  • Surgery affecting hands where pulse oximetry and galvanic skin reaction are recorded or areas where facial muscle activity is measured

  • Any diagnosed condition affecting central nervous system, facial nerves or muscles.

  • Significant facial hair growth in the area where the sensors will be attached

  • Tattoos in the area where the sensors will be attached

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Turku Turku Finland 20140

Sponsors and Collaborators

  • University of Turku
  • Academy of Finland
  • Turku University Hospital

Investigators

  • Principal Investigator: Sanna Salanterä, Prof, University of Turku

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sanna Salanterä, Professor, University of Turku
ClinicalTrials.gov Identifier:
NCT03061240
Other Study ID Numbers:
  • 29092016
First Posted:
Feb 23, 2017
Last Update Posted:
Dec 24, 2018
Last Verified:
Dec 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sanna Salanterä, Professor, University of Turku

Study Results

No Results Posted as of Dec 24, 2018