Publications by authors named "Leonard A Jason"

While research has shown self-beliefs influence recovery from substance use disorder, beliefs about the external world may also be important when considering , or the sum of resources an individual can draw upon to sustain their recovery. Rooted in key concepts of positive psychology and community psychology, recovery capital offers an asset-based framework for understanding recovery as a process of growth to achieve flourishing. This study investigates the role of primal world beliefs, a taxonomy of fundamental beliefs about the world, as they relate to recovery capital in individuals recovering from substance use disorder.

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Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Post-Acute Sequelae of COVID-19 (PASC) often have neurocognitive complaints that involve memory and concentration problems and difficulties paying attention. Other neurocognitive domains such as hypersensitivity to noise and light have rarely been included as aspects of neurocognitive impairment for these post-viral conditions. The current study evaluated a more extensive list of neurocognitive items for a group of 2,313 patients with ME/CFS and 299 patients with PASC.

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Introduction: Safe and stable housing is increasingly recognized as critical to recovery from alcohol and drug use disorders, but research on the outcomes of residents in recovery from opioid use disorder (OUD), particularly those prescribed medications for opioid use disorder (MOUD), is limited.

Methods: This article presents results from an informal survey ( = 15) and discussion with experts in the recovery housing and OUD treatment fields serving as Advisory Board members on the Infrastructure for Studying Treatment and Addiction Recovery Residences (I-STARR) project regarding priorities for research and training on recovery housing for individuals prescribed MOUD. Drawing on the results, we provide a roadmap to establish an evidence base on recovery housing for those prescribed MOUD.

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Background/objectives: Impaired sleep is one of the core symptoms of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), yet the mechanisms and impact of sleep-related issues are poorly understood. Sleep dysfunctions for patients with ME/CFS include frequent napping, difficulties falling asleep, waking up early, and sleep reversal patterns (e.g.

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Individuals involved with the criminal legal system (CLS) face significant challenges upon release from carceral settings, particularly those with substance use disorders (SUD), including opioid overdose rates considerably greater than the general population. Recovery homes play a pivotal role in providing a supportive and stable living environment for individuals reentering the community. However, little is known about recovery homes' ability to assist residents in meeting court-ordered requirements and facilitating connections to community resources.

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Long COVID following SARS-CoV-2 and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) following infectious mononucleosis (IM) are two examples of post-viral syndromes. The identification of risk factors predisposing patients to developing and maintaining post-infectious syndromes may help uncover their underlying mechanisms. The majority of patients with ME/CFS report infectious illnesses before the onset of ME/CFS, with 30% of cases of ME/CFS due to IM caused by the Epstein-Barr virus.

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Recovery homes can provide critical support for individuals taking Medications for Opiate Use Disorders (MOUD). However, some abstinence-based self-help groups and organizations have expressed skepticism toward this harm-reduction strategy. One abstinence-based organization that has welcomed those on MOUD is Oxford House.

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Although the challenges of bereavement among adolescents are well-documented, there is potential for loss to foster growth, development, and positive psychological changes during this developmental period. To examine this possibility, 408 adolescents (46.6% male; 53.

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Background: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) may occur after infection. How often people develop ME/CFS after SARS-CoV-2 infection is unknown.

Objective: To determine the incidence and prevalence of post-COVID-19 ME/CFS among adults enrolled in the Researching COVID to Enhance Recovery (RECOVER-Adult) study.

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Abstinence-specific social support within dyadic relationships is one of the best post-treatment prognostic indicators of recovery and is probably responsible for much of the effectiveness of self-help group participation. Acute treatment after-care in the form of sober-living environments-i.e.

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Recovery homes are located throughout the United States, with the self-governed Oxford Houses representing one of the largest networks with over 3000 homes. Although there is a growing literature on the characteristics and outcomes of these recovery homes, far less is known about differences among the homes. The current study used a set of characteristics that had been proposed by a leader within the Oxford House recovery movement, and a university research team operationalized them into what is now called the Oxford House Stability Questionnaire.

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Article Synopsis
  • The study aimed to determine if individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and a family history of the condition differ from those without such history.
  • A total of 400 ME/CFS patients were examined alongside a control group of patients with multiple sclerosis and post-polio syndrome, revealing significant familial links to ME/CFS.
  • Results showed that 18% of ME/CFS patients had family histories of the condition compared to only 3.9% in the control group and highlighted a correlation between family history and gastrointestinal symptoms in ME/CFS patients.
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The exit from active substance use presents barriers to achieving and maintaining health, especially as individuals lack the economic resources to afford healthcare access. Treatment settings that strengthen resources may support stability in recovery and influence health. Analyzing a sample of recovery home residents over two years (N = 494), the current study assessed individually held resources (e.

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Individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) often experience autonomic symptoms. In the present study, we evaluated 193 adults seeking treatment for ME/CFS, who were recruited from an outpatient clinic. The participants completed a head-up tilt table test to assess two common types of orthostatic intolerance, namely, postural orthostatic tachycardia syndrome (POTS) and orthostatic hypotension (OH).

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There is limited information on the specific impacts of Long COVID in youth. Long COVID presents as persisting or new symptoms following initial COVID-19 infection. The aim of this study was to better understand how children and their families describe their experiences seeking diagnosis and support following the onset of symptoms of Long COVID.

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Spiritually-based interventions in the form of 12-step programs are frequently offered as a part of substance use treatment programs in the United States. Programs based in the 12 steps guarantee that by working their program, an individual will undergo a process of transformation labeled a spiritual awakening. However, the impact of this experience on recovery factors and treatment adherence is unclear.

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Recovery homes are a widespread source of support for those attempting to maintain abstinence. For those who are able to remain in these settings for at least 6 months, outcomes tend to be favorable; however, many leave prematurely. There is a need to better understand the social integration processes that play a major role in giving recovery home residents access to available recovery-related social capital that is associated with better outcomes.

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Long COVID shares a number of clinical features with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), including post-exertional malaise, severe fatigue, and neurocognitive deficits. Utilizing validated assessment tools that accurately and efficiently screen for these conditions can facilitate diagnostic and treatment efforts, thereby improving patient outcomes. In this study, we generated a series of random forest machine learning algorithms to evaluate the psychometric properties of the DePaul Symptom Questionnaire-Short Form (DSQ-SF) in classifying large groups of adults with Long COVID, ME/CFS (without Long COVID), and healthy controls.

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Since 1969, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has been classified as a neurological disease in the International Classification of Diseases by the World Health Organization. Although numerous studies over time have uncovered organic abnormalities in patients with ME/CFS, and the majority of researchers to date classify the disease as organic, many physicians still believe that ME/CFS is a psychosomatic illness. In this article, we show how detrimental this belief is to the care and well-being of affected patients and, as a consequence, how important the education of physicians and the public is to stop misdiagnosis, mistreatment, and stigmatization on the grounds of incorrect psychosomatic attributions about the etiology and clinical course of ME/CFS.

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Purpose: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic disease characterized by substantial fatigue, postexertional malaise, unrefreshing sleep, and orthostatic intolerance, among other symptoms. Specific risk factors for the development of ME/CFS have not been adequately characterized. It has been suggested that ME/CFS is a connective tissue disorder and that joint hyperflexibility is a risk factor for the development of ME/CFS.

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A subset of patients with post-COVID-19 condition (PCC) fulfill the clinical criteria of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). To establish the diagnosis of ME/CFS for clinical and research purposes, comprehensive scores have to be evaluated. We developed the Munich Berlin Symptom Questionnaires (MBSQs) and supplementary scoring sheets (SSSs) to allow for a rapid evaluation of common ME/CFS case definitions.

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Aim: Youth who have not recovered from COVID-19 have been referred to as having Post-Acute Sequelae of SARS-CoV-2 Infection (PASC). The goal of this study was to better understand which symptoms persisted since onset of infection and how these symptoms compare to symptoms experienced by those with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Method: A sample of 19 parents who had a child with PASC were recruited using social media to fill out a questionnaire detailing symptoms at two time points.

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Four decades of research in the field of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) have yielded lessons that may be instructive for those devising criteria to better comprehend Post-Acute Sequelae of SARS CoV-2 Infection (PASC) and Long COVID. For instance, substantial effort has been devoted to defining classification systems, operationalizing methods, and developing instruments with adequate reliability and validity in the ME/CFS field. The current article provides guidelines for developing a case definition for Long COVID and discusses the significance of psychometric issues and criterion variance, including how to specify symptoms, and develop thresholds, subtypes, and exclusionary conditions.

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There have been multiple efforts to evaluate the contributions of the field of Community Psychology, and one of the more popular methods has involved gathering citations and articles published in Community Psychology journals. In recent years, several sites have gathered citation analysis and article publication rates so that it is now relatively easy to summarize settings and scholar rankings. In the current study, articles published in the two major journals of the field of Community Psychology over the past five decades were evaluated for these publications and citations.

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