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Digital Solutions for Concussion

NCT05635656 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2024-09-19

No results posted yet for this study

Summary

The objective of this study is to develop new digital solutions for patients with prolonged postconcussion symptoms, and investigate its usability, feasibility, and safety. The digital solutions consist of a 1) symptom mapping and clinical decision support system, and 2) a research-based system for home-based biofeedback treatment.

Conditions

  • Post-Concussion Syndrome
  • Post-Traumatic Headache

Interventions

DEVICE

Digital symptom mapping and biofeedback treatment

Digital symptom mapping and biofeedback treatment

Sponsors & Collaborators

  • St. Olavs Hospital

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-25
Primary Completion
2024-03-05
Completion
2024-03-05

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05635656 on ClinicalTrials.gov