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eHealth cognitive rehabilitation for brain tumor patients: results of a randomized controlled trial.
van der Linden, Sophie D; Rutten, Geert-Jan M; Dirven, Linda; Taphoorn, Martin J B; Satoer, Djaina D; Dirven, Clemens M F; Sitskoorn, Margriet M; Gehring, Karin.
Afiliação
  • van der Linden SD; Department of Neurosurgery, Elisabeth-TweeSteden Hospital, Tilburg, the Netherlands.
  • Rutten GM; Department of Cognitive Neuropsychology, Tilburg University, Room S219, P.O. Box 90153, 5000 LE, Tilburg, the Netherlands.
  • Dirven L; Department of Neurosurgery, Elisabeth-TweeSteden Hospital, Tilburg, the Netherlands.
  • Taphoorn MJB; Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
  • Satoer DD; Department of Neurology, Haaglanden Medical Center, The Hague, the Netherlands.
  • Dirven CMF; Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
  • Sitskoorn MM; Department of Neurology, Haaglanden Medical Center, The Hague, the Netherlands.
  • Gehring K; Department of Neurosurgery, Erasmus Medical Center, Rotterdam, the Netherlands.
J Neurooncol ; 154(3): 315-326, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34487313
ABSTRACT

BACKGROUND:

Evidence-based cognitive rehabilitation programs for brain tumor patients are not widely available, despite the high need. We aimed to evaluate the effects of a tablet-based cognitive rehabilitation program on cognitive performance, cognitive complaints, fatigue, and psychological distress in primary brain tumor patients following neurosurgery. Also, attrition, adherence and patient satisfaction with the program were evaluated.

METHODS:

Adults with presumed low-grade glioma and meningioma were recruited before surgery. Three months thereafter, participants were allocated to the intervention group or waiting-list control group using minimization. The 10-week eHealth app ReMind, based on the effective face-to-face intervention, consisted of psychoeducation, strategy-training and attention retraining. Performance-based cognitive outcomes and patient-reported outcomes were assessed before surgery and 3, 6 and 12 months thereafter. Mean scores, percentages of cognitively impaired individuals and reliable change indices (RCIs) were compared between groups.

RESULTS:

Sixty-two out of 183 eligible patients were randomized. Of the people who declined, 56% reported that participation would to be too burdensome. All participants found a tablet-app suitable for delivery of cognitive rehabilitation and 90% rated the program as "good" or "excellent". Performance-based cognitive outcomes and patient-reported outcomes did not significantly differ in group means over time nor RCIs between the intervention (final n = 20) and control group (final n = 25).

CONCLUSIONS:

Recruitment at this early stage was difficult, resulting in limited statistical power. No significant effects were demonstrated, while adherence and satisfaction with the eHealth program were good. In clinical practice, ReMind may be helpful, if timing would be adapted to patients' needs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article