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All participants will sign the informed consent prior to enrollment in the baseline visit. The informed consent will be available from the corresponding author upon request. Details of the design of the trial can be also gathered from Supplementary Material (Standard Protocol Items: Recommendations for Interventional Trials [SPIRIT] Checklist and Schedule of enrolment, interventions and assessments [SPIRIT] Flow diagram). The trial is registered at ClinicalTrials.gov, identifier: NCT04084795 (2nd of August of 2019).","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"Not applicable.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"BLA was the Research Committee Chair of EMDR Europe between 2017 and 2021 and has been invited as speaker to various national and international congresses of EMDR. AVG is member of the Research Committee of EMDR Europe since May 2023 until now. AMA is member of the Research Committee of the Spanish EMDR Organization since September 2023 until now. The other authors declare they have no competing interests.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"856"}}