Semi-Automated Neurofeedback Therapy for Persistent Postconcussive Symptoms in a Military Clinical Setting: A Feasibility Study.
Autor: | Hershaw JN; Defense and Veterans Brain Injury Center, Building 7489, Sutherland Circle, Fort Carson, Colorado 80913., Hill-Pearson CA; Defense and Veterans Brain Injury Center, Building 7489, Sutherland Circle, Fort Carson, Colorado 80913., Arango JI; Defense and Veterans Brain Injury Center, Building 7489, Sutherland Circle, Fort Carson, Colorado 80913., Souvignier AR; Defense and Veterans Brain Injury Center, Building 7489, Sutherland Circle, Fort Carson, Colorado 80913.; Warrior Recovery Center, Evans Army Community Hospital, Fort Carson, Colorado 80913., Pazdan RM; Defense and Veterans Brain Injury Center, Building 7489, Sutherland Circle, Fort Carson, Colorado 80913.; Warrior Recovery Center, Evans Army Community Hospital, Fort Carson, Colorado 80913. |
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Jazyk: | angličtina |
Zdroj: | Military medicine [Mil Med] 2020 Mar 02; Vol. 185 (3-4), pp. e457-e465. |
DOI: | 10.1093/milmed/usz335 |
Abstrakt: | Introduction: Neurofeedback therapy (NFT) has demonstrated effectiveness for reducing persistent symptoms following traumatic brain injury (TBI); however, its reliance on NFT experts for administration and high number of treatment sessions limits its use in military medicine. Here, we assess the feasibility of live Z-score training (LZT)-a variant of NFT that requires fewer treatment sessions and can be administered by nonexperts-for use in a military clinical setting. Materials and Methods: A single group design feasibility study was conducted to assess acceptability, tolerance, treatment satisfaction, and change in symptoms after a 6-week LZT intervention in 38 Service Members (SMs) with persistent symptoms comorbid with or secondary to mild TBI. Acceptance and feasibility were assessed using treatment completion and patients' satisfaction with treatment. To evaluate changes in symptom status, a battery of self-report questionnaires was administered at baseline, posttreatment, and 3-month follow-up to evaluate changes in psychological, neurobehavioral, sleep, pain, and headache symptoms, as well as self-efficacy in symptom management and life satisfaction. Results: Participants tolerated the treatment well and reported a positive experience. Symptom improvement was observed, including depressive, neurobehavioral, and pain-related symptoms, with effects sustained at 3-month follow-up. Conclusion: LZT treatment appears to be a feasible, non-pharmacological therapy amenable to SMs. Results from this pilot study promote further investigation of LZT as an intervention for SMs with persistent symptoms following TBI. (© Association of Military Surgeons of the United States 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.) |
Databáze: | MEDLINE |
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