Cognitive Frailty and Oxygen-ozone Therapy

December 22, 2023 updated by: Cristian Bonvicini, IRCCS Centro San Giovanni di Dio Fatebenefratelli

Cognitive Frailty and Oxygen-ozone Therapy: Integrated Approach to Identify Biological and Neuropsychological Markers

As the world's population age, frailty is moving to the forefront of health and medical research and may become one of the world's most serious health issues. Understanding frailty prevention and treatment becomes even more crucial in order to reduce national healthcare costs. Oxygen-Ozone (O2-O3) therapy is a no-invasive/no-pharmacological and low cost procedure based on the therapeutic effects of low O3 concentrations, already used in medicine as an alternative/adjuvant treatment for different diseases and in the elderly. This project is the first pilot double blind randomized controlled trial where a group of elderly frail subjects are stratified as untreated (air), treated with pure O2 and treated with a mixture of O2-O3. The biological corollary will be transcriptomics, proteomics and also cognitive impairment assessment at baseline and after treatment. An algorithm combining these data will identify biomarkers of the response to O2-O3 therapy.

Study Overview

Detailed Description

Background: Although frailty does not yet have an internationally recognized standard definition, the general premise is that it may be considered a geriatric syndrome reflecting multi-system dysfunction, in which individuals are able to dynamically transition between severity states. The World Health Organization and The International Association of Geriatrics and Gerontology are working on an internationally accepted frailty definition. Accumulating evidence supports the existence of a close relation between frailty and cognitive impairment in subjects with/without dementia. To date specific treatments for the cognitive frailty are not still available. Oxygen-Ozone (O2-O3) therapy is a no-invasive/no-pharmacological low cost procedure based on therapeutic effects of low O3 concentrations and used in medicine as an alternative/adjuvant treatment for different diseases and for improving metabolic activities in elderly. Molecular evidence shows that low O3 concentrations dissolve in the biological fluids and induce a mild oxidative stress, which stimulates antioxidant defences thus preventing the inflammatory response and cell damage. Inflammatory processes, altered release of the main reactive O2 species and mitochondrial/cytoskeletal modifications have been hypothesized to influence significantly the frailty state as well as the neurodevelopmental network on cognitive impairment.

Aims

  1. To characterize clinical and neuropsychological-cognitive impairment profiles in elderly frail subjects at baseline and after treatment.
  2. To identify in vivo peripheral biomarkers associated to O2-O3 therapy through transcriptomic and proteomic analyses at baseline and after treatment.
  3. To correlate clinical/cognitive improvement with transcriptomic and proteomic profiles to identify biomarkers associated to treatment response.

Study Type

Interventional

Enrollment (Actual)

75

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Brescia, Italy, 25125
        • IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. subjects between the ages of 60 and 85, referring to the diagnosis of amnesic or non-amnesic cognitive disorder, reported by the subject himself or by family members;
  2. MMSE score > 24/30;
  3. exclusion of dementia, even in the presence of ascertained Alzheimer's disease detected by the most advanced diagnostic techniques;
  4. function intact, or functional reduction not related to the cognitive problem;
  5. pharmacological therapy for the treatment of stable cognitive or behavioral disorders for at least 3 months at the time of enrolment;
  6. specific assessments/tools for frailty: "Italian frailty index (IFi)" and for "Frailty Instrument (FIt) based on the Survey of Health, Ageing and Retirement in Europe (SHARE-FIt)".

Exclusion Criteria:

  1. subjects affected by disabling vision or hearing impairments;
  2. subjects affected by known psychosis or psychiatric illness, alcohol or drug abuse;
  3. subjects affected by uncontrolled hyperthyroidism or by Glucose-6-Phostate Dehydrogenase Deficiency (G6PD)-Favism (according to S.I.O.O.T Guidelines, http://www.ossiozono.it);
  4. subjects who considered invasive the methodology for rectal insufflation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Oxygen-Ozone (O2-O3)
A small catheter is inserted into the rectum and a total amount of 150cc of O2-O3 mixture at the concentration of 30ug of O3 per cc of O2 over a 5-10 min period is administered.
Oxygen-Ozone (O2-O3) treatment by rectal insufflations for 5 weeks (3 sessions for week).
Active Comparator: Oxygen (O2)
A small catheter is inserted into the rectum and a total amount of 150cc of O2 over a 5-10 min period is administered.
Oxygen (O2) treatment by rectal insufflations for 5 weeks (3 sessions for week).
Placebo Comparator: Placebo (Air)
A small catheter is inserted into the rectum and a total amount of 150cc of air over a 5-10 min period is administered.
Air treatment by rectal insufflations for 5 weeks (3 sessions for week).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline and post-intervention in Italian frailty index (IFi)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Italian frailty index (IFi) is an Italian version of the "frailty index" based on accumulation of age-related deficits. IFi has been expressed as a ratio of deficits present/deficits considered after a comprehensive geriatric assessment.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Frailty Instrument (FIt) based on the Survey of Health, Ageing and Retirement in Europe (SHARE-FIt)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

SHARE-FIt is based on 5-item (i.e. grip strength and four self-reported items: fatigue, loss of appetite and/or eating less than usual, difficulties climbing stairs and/or walking 100 metres, and low level of physical activity). For each gender, a discreet factor (DFactor) model was estimated based on the five SHARE frailty variables.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Everyday Memory Questionnaire (EMQ)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Everyday Memory Questionnaire (EMQ) is a subjective measure of memory failure in everyday life, lower scores indicating better memory function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Raven's Progressive Matrices (RPM)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Raven's Progressive Matrices (RPM) is used to measure fluid intelligence, with higher scores indicating better function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Free and Cued Selective Reminding Test (FCSRT)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Free and Cued Selective Reminding Test (FCSRT) is a test used to assess episodic memory, with higher scores indicating better function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Rey-Osterrieth Complex Figure A Test (ROCF-A)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

ROCF-A is used to explore visuo-constructional ability and visuo-spatial memory, with higher scores indicating better function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Face-name association task (FNAT)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

FNAT is used to assess the patient's associative memory and is composed of encoding and retrieval phases, with higher scores indicating better function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Picture naming task (PNT)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

The PNT is designed to explore lexical access, with higher scores indicating better function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Trail Making Tests A (TMT-A)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Trail Making Tests A (TMT-A) is used to assess visual attention and motor speed skills, with lower scores indicating better attention.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in Trail Making Tests B (TMT-B)
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Trail Making Tests B (TMT-B) is used to assess executive functions, with lower scores indicating good performance in executive function.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline and post-intervention in peripheral mRNAs levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

The mRNAs peripheral signatures compared before and after treatments. To identify the list of differentially expressed mRNAs we filter ANOVA results using both fold change |FC| ≥ 1.5 and p-value ≤0.05.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral NGFb (beta-Nerve Growth Factor) levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of NGFb compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral BDNF (Brain Derived Neurotrophic Factor) levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of BDNF compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral VEGF (Vascular Endothelial Growth Factor) levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of VEGF compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-1b levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-1b compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-4 levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-4 compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-6 levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-6 compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-8 levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-8 compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-9 levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-9 compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-10 levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-10 compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IL, Interleukin-13 levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IL-13 compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral TNF-a (Tumor Necrosis Factor) levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of TNF-a compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)
Change from baseline and post-intervention in peripheral IFN-g (Interferon-gamma) levels in subjects stratified according to IFi or SHARE-FIt scores
Time Frame: Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Peripheral concentrations (pg/ml) of IFN-g compared before and after treatments.

Change = month 3rd after treatment - baseline score / Change = month 9th after treatment - baseline score / Change = month 15th after treatment - baseline score

Baseline (pre-intervention), post-intervention (3, 9 and 15 months)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Cristina Geroldi, MD, IRCCS Centro San Giovanni di Dio Fatebenefratelli

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 2, 2019

Primary Completion (Actual)

November 2, 2022

Study Completion (Actual)

November 17, 2023

Study Registration Dates

First Submitted

September 11, 2023

First Submitted That Met QC Criteria

October 2, 2023

First Posted (Actual)

October 6, 2023

Study Record Updates

Last Update Posted (Actual)

December 26, 2023

Last Update Submitted That Met QC Criteria

December 22, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RF-2016-02363298

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Cognitive Frailty

Clinical Trials on Experimental: Oxygen-Ozone (O2-O3)

Subscribe