Cognitive Profile of Patients at the Sagol Center for Hyperbaric Medicine and Research

NCT04287283 · tracked via the Priya Life Science Israel tracker

Sponsor

Assaf-Harofeh Medical Center

Phase

Observational

Started

2008-01

Last updated

2026-04-21

Condition(s) studied

TBI (Traumatic Brain Injury)StrokeFibromyalgiaAging

Investigational drug(s) / intervention(s)

Hyperbaric Oxygen

Hyperbaric Oxygen: 40-60 daily hyperbaric sessions, 5 days per week. Each session consists of 90 minutes exposure to 100% oxygen at 1.5-2 ATA.

Study summary

In the investigator's institute there is ongoing treatment of different patients with cognitive deficits using Hyperbaric oxygen therapy (HBOT). These patients undergo neuro-cognitive function computerized tests before and after treatment.

The aim of this study was to retrospectively evaluate the cognitive changes before and after HBOT in different patients populations.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Patients included if they completed at least two neuro-cognitive computerized tests, before and after HBOT Exclusion Criteria: * Patients who were not able to complete two cognitive tests

Primary outcome measure(s)

Change in neurocognitive scores — baseline and 12 weeks
change in scores in a computerized neuro-cognitive test, "IQ-scale" score, normalized for age and education, with mean=100 and SD=15 points in healthy population, higher score implies better results.

Trial sites (1)

Facility	City	Region	Status
hyperbaric center Asaf harofe medical center	Rishon LeZiyyon	Israel

More Assaf-Harofeh Medical Center trials in Israel

Effect of Hyperoxygenated Environment on Maximal Muscle Strength Recruiting

Sensory Rehabilitation in Chemo Induced Peripheral Neuropathy Recruiting

Metabolic Changes Associated With Weight Gain After Treatment of Achalasia Starting soon

Hyperbaric Oxygen Therapy Used on Severely Injured Healthy Individuals With Fungal Infections Active, not recruiting

Tranexamic Acid During Colonic Endoscopic Resection Procedures Recruiting

Other trials for the same condition

Carotid Artery Implant for Preventing Stroke in Atrial Fibrillation Patients Taking Oral Anticoagulants Active, not recruiting

The Efficacy of Additional Motor Training Dosage During the Early Stages Post Stroke on the Upper Extremity Recovery Recruiting

Fecal Microbiome Transplantation From Healthy Donors to Individuals With Fibromyalgia Enrolling by invitation

AMPLATZER PFO Occluder Post Approval Study Active, not recruiting

The Effect of Remote Electrical Neuromodulation (REN) on Conditioned Pain Modulation (CPM) in Migraine and Fibromyalgia Recruiting

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04287283 on ClinicalTrials.gov ↗ ← All trials in Israel