Cognitive behavioral therapy, exercise training, and cognitive remediation for patients with post-COVID-19 condition: protocol of an open-label randomized controlled trial
Year: 2025
Type: article
Study design: Study Protocol
Abstract: BACKGROUND: Effective rehabilitation programs targeting transdiagnostic mechanisms of persistent physical symptoms are needed in long COVID. We present a transparency-focused description of the protocol of an open-label randomized controlled trial designed to evaluate the efficacy and tolerance of a multidisciplinary intensive rehabilitation program versus usual care. METHODS: After a day-hospital multidisciplinary evaluation program including minimal psychoeducation and personalized recommendations, patients presenting with persistent symptoms after COVID-19 are proposed to participate to the study. The intervention consists of a 6-week rehabilitation program with groups of 3 to 5 patients attending three day-hospital sessions per week. The rehabilitation program combines adapted physical activity (three sessions per week with progressive exertion thresholds), cognitive remediation (two computer-based personalized sessions per week) and cognitive behavioral therapy (CBT, two sessions per week: one group session and one individual session). CBT sessions encompass psychoeducation, cognitive restructuring, behavioral activation and gradual exposure, and problem-solving skills. Our primary outcome is health-related quality of life (HRQoL) at 6 months, measured with the Physical Component Score (PCS) of the 12-item Short-Form Health Survey. The secondary outcomes are the Mental Component Score (MCS) at 6 months, PCS and MCS at 3 months, the main persistent symptoms (fatigue, dyspnea, cognitive complaints, pain) and associated psychological burden at 3 and 6 months, and patients’ satisfaction at 3 months. All included patients undergo an inclusion visit including a physical condition evaluation, a neuropsychological assessment, a first consultation with the CBT therapist, and the completion of several questionnaires for the secondary outcomes (Pichot scale, Borg scale, Cognitive Difficulties Scale, pain numeric scale, and Somatic Symptom disorder-B criteria scale). These evaluations are repeated at 3- and 6-month follow-up. All analyses will be performed in intention to treat following CONSORT Statement recommendations. DISCUSSION: Our goal is to demonstrate that a multidisciplinary intensive rehabilitation program combining adapted physical activity, cognitive remediation, and CBT leads to an improvement in HRQoL in the long term (i.e., six months after a multidisciplinary evaluation program including minimal psychoeducation and personalized recommendations) in patients with long COVID, while being feasible, acceptable, and safe. TRIAL REGISTRATION: NCT number NCT05532904, registration date: 2022–09-07.
Source: BMC Psychology
Authors: Clément Gouraud, Agathe Ancellin-Geay, Corentin Verot, Isabelle Bergeras, Laura Poudevigne, Lucile Cormier, Séverine Gilbert, Frédéric Limosin, Laurence Lacoste, Diane Ribayrol, Charles Ouazana Vedrines, Victor Pitron, Karima Mesbahi-Ihadjadene, Hendy Abdoul, Jessica Rousseau, Alexandra Kachaner, Brigitte Ranque, Patricia Thoreux, Cédric Lemogne
Institutions: Assistance Publique – Hôpitaux de Paris, Hôtel-Dieu de Paris, Hôpital Corentin-Celton, Inserm, Université Paris Cité, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement, Université Sorbonne Paris Nord, Centre de Recherche Épidémiologie et Statistique, Sommeil, vigilance, fatigue et santé publique, Hôpital Cochin, Pharmacologie et évaluation thérapeutiques chez l'enfant et la femme enceinte, Hôpital Européen Georges-Pompidou
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,990
Award: G5367274965
OpenAlex ID: W4417449297
