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Biofeedback as an intervention for persistent post-concussive symptoms: A randomized feasibility trial
Background Case reports indicate that low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback may improve physiological functioning in individuals with persistent post-concussive symptoms. However, it is unclear whether larger-scale studies are feasible. Purpos...
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Published in: | Journal of concussion 2021-01, Vol.5 |
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container_title | Journal of concussion |
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creator | Bonn, Marquise M Alvarez, Liliana Graham, Laura Thompson, James W Dickey, James P |
description | Background
Case reports indicate that low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback may improve physiological functioning in individuals with persistent post-concussive symptoms. However, it is unclear whether larger-scale studies are feasible.
Purpose
To evaluate the feasibility of a combined low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback intervention for individuals with persistent post-concussive symptoms.
Methods
Individuals with persistent post-concussive symptoms were randomized into intervention and control groups, and their baseline and post-test assessments were compared to a healthy control group. Outcomes included self-report questionnaires, resting electroencephalograph and electrocardiograph recordings, and a driving simulation task. Participants in the intervention group completed three 20 min low-resolution electromagnetic tomography neurofeedback sessions per week and at-home heart rate variability biofeedback training every morning and night for 8 weeks. Feasibility was evaluated according to recruitment capability and sample characteristics, data collection procedures, suitability of the intervention and study procedures, management and implementation of the study intervention, and preliminary participant responses to the intervention.
Results
Thirty-three individuals were recruited and 24 completed this study (seven intervention participants, nine persistent post-concussive symptoms control participants, and eight healthy control participants). One-quarter of participants (four intervention participants and three persistent post-concussive symptoms control participants) experienced simulator sickness during the driving simulator task and had to withdraw from the study. Intervention participants had an 88% and 86% compliance rate for the low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback sessions, respectively. Low-resolution electromagnetic tomography neurofeedback sessions took approximately 1 h to complete per participant. Preliminary analysis indicated that the intervention reduced electroencephalograph z-score deviation with a very large effect size (d = 1.36) compared to the other study groups.
Conclusions
Pilot studies evaluating the efficacy of low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback should be performed to confirm these preliminary findin |
doi_str_mv | 10.1177/20597002211046459 |
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Case reports indicate that low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback may improve physiological functioning in individuals with persistent post-concussive symptoms. However, it is unclear whether larger-scale studies are feasible.
Purpose
To evaluate the feasibility of a combined low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback intervention for individuals with persistent post-concussive symptoms.
Methods
Individuals with persistent post-concussive symptoms were randomized into intervention and control groups, and their baseline and post-test assessments were compared to a healthy control group. Outcomes included self-report questionnaires, resting electroencephalograph and electrocardiograph recordings, and a driving simulation task. Participants in the intervention group completed three 20 min low-resolution electromagnetic tomography neurofeedback sessions per week and at-home heart rate variability biofeedback training every morning and night for 8 weeks. Feasibility was evaluated according to recruitment capability and sample characteristics, data collection procedures, suitability of the intervention and study procedures, management and implementation of the study intervention, and preliminary participant responses to the intervention.
Results
Thirty-three individuals were recruited and 24 completed this study (seven intervention participants, nine persistent post-concussive symptoms control participants, and eight healthy control participants). One-quarter of participants (four intervention participants and three persistent post-concussive symptoms control participants) experienced simulator sickness during the driving simulator task and had to withdraw from the study. Intervention participants had an 88% and 86% compliance rate for the low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback sessions, respectively. Low-resolution electromagnetic tomography neurofeedback sessions took approximately 1 h to complete per participant. Preliminary analysis indicated that the intervention reduced electroencephalograph z-score deviation with a very large effect size (d = 1.36) compared to the other study groups.
Conclusions
Pilot studies evaluating the efficacy of low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback should be performed to confirm these preliminary findings. However, the protocol should be modified to reduce participant fatigue and withdrawal. This trial was registered with Clinicialtrials.gov (NCT03338036; https://clinicaltrials.gov/ct2/show/NCT03338036?term=03338036&draw=2&rank=1).</description><identifier>ISSN: 2059-7002</identifier><identifier>EISSN: 2059-7002</identifier><identifier>DOI: 10.1177/20597002211046459</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Biofeedback ; Case reports ; EEG ; Feedback ; Heart rate ; Tomography</subject><ispartof>Journal of concussion, 2021-01, Vol.5</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is licensed under the Creative Commons Attribution License https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2009-c7785e6069f9c774f10aea8bd54d8fabfbdcee70ff863e73fa1108d7702652bf3</citedby><cites>FETCH-LOGICAL-c2009-c7785e6069f9c774f10aea8bd54d8fabfbdcee70ff863e73fa1108d7702652bf3</cites><orcidid>0000-0002-4101-835X ; 0000-0002-2097-6786 ; 0000-0003-0809-9618</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2612345404?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25751,27922,27923,37010,44588</link.rule.ids></links><search><creatorcontrib>Bonn, Marquise M</creatorcontrib><creatorcontrib>Alvarez, Liliana</creatorcontrib><creatorcontrib>Graham, Laura</creatorcontrib><creatorcontrib>Thompson, James W</creatorcontrib><creatorcontrib>Dickey, James P</creatorcontrib><title>Biofeedback as an intervention for persistent post-concussive symptoms: A randomized feasibility trial</title><title>Journal of concussion</title><description>Background
Case reports indicate that low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback may improve physiological functioning in individuals with persistent post-concussive symptoms. However, it is unclear whether larger-scale studies are feasible.
Purpose
To evaluate the feasibility of a combined low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback intervention for individuals with persistent post-concussive symptoms.
Methods
Individuals with persistent post-concussive symptoms were randomized into intervention and control groups, and their baseline and post-test assessments were compared to a healthy control group. Outcomes included self-report questionnaires, resting electroencephalograph and electrocardiograph recordings, and a driving simulation task. Participants in the intervention group completed three 20 min low-resolution electromagnetic tomography neurofeedback sessions per week and at-home heart rate variability biofeedback training every morning and night for 8 weeks. Feasibility was evaluated according to recruitment capability and sample characteristics, data collection procedures, suitability of the intervention and study procedures, management and implementation of the study intervention, and preliminary participant responses to the intervention.
Results
Thirty-three individuals were recruited and 24 completed this study (seven intervention participants, nine persistent post-concussive symptoms control participants, and eight healthy control participants). One-quarter of participants (four intervention participants and three persistent post-concussive symptoms control participants) experienced simulator sickness during the driving simulator task and had to withdraw from the study. Intervention participants had an 88% and 86% compliance rate for the low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback sessions, respectively. Low-resolution electromagnetic tomography neurofeedback sessions took approximately 1 h to complete per participant. Preliminary analysis indicated that the intervention reduced electroencephalograph z-score deviation with a very large effect size (d = 1.36) compared to the other study groups.
Conclusions
Pilot studies evaluating the efficacy of low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback should be performed to confirm these preliminary findings. However, the protocol should be modified to reduce participant fatigue and withdrawal. This trial was registered with Clinicialtrials.gov (NCT03338036; https://clinicaltrials.gov/ct2/show/NCT03338036?term=03338036&draw=2&rank=1).</description><subject>Biofeedback</subject><subject>Case reports</subject><subject>EEG</subject><subject>Feedback</subject><subject>Heart rate</subject><subject>Tomography</subject><issn>2059-7002</issn><issn>2059-7002</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1UE1Lw0AUXETBUvsDvC14Tn272WQTb7X4BQUveg6b5K1sbbJx37ZQf70pFRTE0xuGmXnMMHYpYC6E1tcSslIDSCkEqFxl5QmbHLjkQJ7-wudsRrQGAFFoLRVMmL113iK2tWneuSFueu76iGGHfXS-59YHPmAgR3Fk-OApJo3vmy2R2yGnfTdE39ENX_Bg-tZ37hNbbtGQq93GxT2PwZnNBTuzZkM4-75T9np_97J8TFbPD0_LxSppJECZNFoXGeaQl7YcsbICDJqibjPVFtbUtm4bRA3WFnmKOrVmbFy0WoPMM1nbdMqujrlD8B9bpFit_Tb048tK5kKmKlOgRpU4qprgiQLaagiuM2FfCagOi1Z_Fh0986OHzBv-pP5v-AK91Xc1</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Bonn, Marquise M</creator><creator>Alvarez, Liliana</creator><creator>Graham, Laura</creator><creator>Thompson, James W</creator><creator>Dickey, James P</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-4101-835X</orcidid><orcidid>https://orcid.org/0000-0002-2097-6786</orcidid><orcidid>https://orcid.org/0000-0003-0809-9618</orcidid></search><sort><creationdate>20210101</creationdate><title>Biofeedback as an intervention for persistent post-concussive symptoms: A randomized feasibility trial</title><author>Bonn, Marquise M ; Alvarez, Liliana ; Graham, Laura ; Thompson, James W ; Dickey, James P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2009-c7785e6069f9c774f10aea8bd54d8fabfbdcee70ff863e73fa1108d7702652bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biofeedback</topic><topic>Case reports</topic><topic>EEG</topic><topic>Feedback</topic><topic>Heart rate</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonn, Marquise M</creatorcontrib><creatorcontrib>Alvarez, Liliana</creatorcontrib><creatorcontrib>Graham, Laura</creatorcontrib><creatorcontrib>Thompson, James W</creatorcontrib><creatorcontrib>Dickey, James P</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Journal of concussion</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonn, Marquise M</au><au>Alvarez, Liliana</au><au>Graham, Laura</au><au>Thompson, James W</au><au>Dickey, James P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biofeedback as an intervention for persistent post-concussive symptoms: A randomized feasibility trial</atitle><jtitle>Journal of concussion</jtitle><date>2021-01-01</date><risdate>2021</risdate><volume>5</volume><issn>2059-7002</issn><eissn>2059-7002</eissn><abstract>Background
Case reports indicate that low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback may improve physiological functioning in individuals with persistent post-concussive symptoms. However, it is unclear whether larger-scale studies are feasible.
Purpose
To evaluate the feasibility of a combined low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback intervention for individuals with persistent post-concussive symptoms.
Methods
Individuals with persistent post-concussive symptoms were randomized into intervention and control groups, and their baseline and post-test assessments were compared to a healthy control group. Outcomes included self-report questionnaires, resting electroencephalograph and electrocardiograph recordings, and a driving simulation task. Participants in the intervention group completed three 20 min low-resolution electromagnetic tomography neurofeedback sessions per week and at-home heart rate variability biofeedback training every morning and night for 8 weeks. Feasibility was evaluated according to recruitment capability and sample characteristics, data collection procedures, suitability of the intervention and study procedures, management and implementation of the study intervention, and preliminary participant responses to the intervention.
Results
Thirty-three individuals were recruited and 24 completed this study (seven intervention participants, nine persistent post-concussive symptoms control participants, and eight healthy control participants). One-quarter of participants (four intervention participants and three persistent post-concussive symptoms control participants) experienced simulator sickness during the driving simulator task and had to withdraw from the study. Intervention participants had an 88% and 86% compliance rate for the low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback sessions, respectively. Low-resolution electromagnetic tomography neurofeedback sessions took approximately 1 h to complete per participant. Preliminary analysis indicated that the intervention reduced electroencephalograph z-score deviation with a very large effect size (d = 1.36) compared to the other study groups.
Conclusions
Pilot studies evaluating the efficacy of low-resolution electromagnetic tomography neurofeedback and heart rate variability biofeedback should be performed to confirm these preliminary findings. However, the protocol should be modified to reduce participant fatigue and withdrawal. This trial was registered with Clinicialtrials.gov (NCT03338036; https://clinicaltrials.gov/ct2/show/NCT03338036?term=03338036&draw=2&rank=1).</abstract><cop>London, England</cop><pub>SAGE Publications</pub><doi>10.1177/20597002211046459</doi><orcidid>https://orcid.org/0000-0002-4101-835X</orcidid><orcidid>https://orcid.org/0000-0002-2097-6786</orcidid><orcidid>https://orcid.org/0000-0003-0809-9618</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biofeedback Case reports EEG Feedback Heart rate Tomography |
title | Biofeedback as an intervention for persistent post-concussive symptoms: A randomized feasibility trial |
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