After traumatic experiences, intrusive memories can flash back and evoke significant distress. Here, we investigated whether the frequency and severity of intrusions can be reduced by the provision of placebo. After the (online) exposure to the trauma-film paradigm, healthy participants (N = 112) received deceptive placebo (DP), open-label placebo (OLP), or no treatment. In the DP group, participants were led to believe to receive a dopamine-modulating drug, which was supposed to disrupt the consolidation of traumatic memories, although they in fact received the same placebo tablets as the OLP group for one week. The results show that the groups did not differ in the frequency of intrusive memories after one week. However, participants receiving OLP reported a significantly reduced intensity of intrusions as compared to DP. Across groups, negative expectations about the intensity and controllability of intrusions were associated with a higher frequency of intrusions, higher distress, higher burden, and more negative appraisal. The results suggest that expectations play an important role in the emergence of intrusive memories and that some of the disabling aspects of intrusive memories can be reduced by placebo. This may carry clinical potential because placebos are an accessible, cost-effective intervention to reduce the risk of intrusive memories.
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http://dx.doi.org/10.1016/j.brat.2022.104197 | DOI Listing |
Front Psychol
December 2024
War Related Illness and Injury Study Center, VA Palo Alto Health Care System, Palo Alto, CA, United States.
Eur J Psychotraumatol
December 2024
Department of Clinical Psychology and Psychological Therapies, Norwich Medical School, University of East Anglia, Norwich, UK.
PTSD is comorbid with a number of other mental health difficulties and the link between voice hearing and PTSD has been explored in adult samples. To compare the trauma history, symptomatology, and cognitive phenotypes of children and adolescents with a PTSD diagnosis following exposure to multiple traumatic events presenting with voice hearing with those who do not report hearing voices. Participants ( = 120) were aged 8-17 years and had PTSD following exposure to multiple traumas.
View Article and Find Full Text PDFBurns
December 2024
Graduate Institute of Behavioral Sciences, Chang Gung University, Taoyuan, Taiwan; Department of Psychiatry, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan. Electronic address:
Objective: Burn injuries can be traumatic and lead to psychological sequelae, particularly acute stress disorder (ASD). Information regarding the prevalence and risk factors of ASD following DSM-5 criteria is relatively limited among survivors of burn and other traumas. This study aimed to investigate the prevalence of probable ASD post-burn according to DSM-5 criteria and explore the impact and interplay of pre- and peri-trauma psychological risk factors on DSM-5 ASD symptomatology.
View Article and Find Full Text PDFExp Brain Res
December 2024
Department of Psychology, University of Otago, Dunedin, New Zealand.
Memory intrusion is a characteristic of posttraumatic stress disorder manifesting as involuntary flashbacks of negative events. Interference of memory reconsolidation using cognitive tasks has been employed as a noninvasive therapy to prevent subsequent intrusive retrieval. The present study aims to test whether physical activity, with its cognitive demands and unique physiological effects, may provide a novel practice to reduce later involuntary retrieval via the reconsolidation mechanism.
View Article and Find Full Text PDFOphthalmology
December 2024
Department of Ophthalmology and Visual Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR; Department of Ophthalmology and Visual Sciences, The Prince of Wales Hospital, Hong Kong SAR; Hong Kong Eye Hospital, Hong Kong SAR; Eye Centre, The Chinese University of Hong Kong Medical Centre, Hong Kong SAR. Electronic address:
Objective: To evaluate the use of virtual reality-based infrared pupillometry (VIP) to detect individuals suffering long COVID.
Design: Prospective, case-control cross-sectional study.
Participants: Participants aged 20-60 were recruited from a community eye screening programme.
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