Abstract:Background
People with aphasia (PWA) report higher levels of stress in comparison to stroke survivors without aphasia. If untreated, chronic stress is known to have detrimental effects to the body and brain and can negatively impact health and well-being. According to extant literature, self- and proxy-report agreement on objective domains is higher than on subjective domains, like chronic stress. In addition, high levels of mutuality, also known as shared feelings between two people, have been str… Show more
“…The most frequently used version of the scale was the PSS-10, found in 7 studies 2,19–24 . The PSS-14 was used less often, followed by the PSS-4 and the modified PSS 3,25–29 . Many studies (9) reported on the type and location of stroke (ie, descriptors including ischemic, hemorrhagic, left hemispheric, or right hemispheric stroke).…”
Section: Resultsmentioning
confidence: 99%
“…The PSS was collected at multiple time points across studies. In cross-sectional studies, collection varied from time of hospital admission to 7 days after stroke, a few months, or even 12 months or greater post stroke 2,3,19,20,25–28 . These studies reported moderate to high levels of PS, ranging from 5.0 for the PSS-4, 14.04 to 16.90 for the PSS-10, and 29.62 for the PSS-14 2,3,19,20,26,28 .…”
Section: Resultsmentioning
confidence: 99%
“…Although there are many additional contributing factors, most works found a correlation between scores in stroke severity and PS. 2,3,19,20,25,26 Worsening neurological deficits (National Institutes of Health Stroke Scale), poor scores on the Stroke Impact Scale, and greater impairment of cognitive function (cognitive FIM) and motor function (motor FIM) were associated with higher levels of PS. 2,3,19,20,25,26 PSS in Cross-sectional Studies.…”
Section: Resultsmentioning
confidence: 99%
“…Stroke is a leading cause of long-term disability, and almost 75% of survivors are left with some degree of physical disability 1 . Consequently, these patients may have to relearn how to perform activities of daily living while simultaneously trying to regain control of emotional and cognitive functions 2,3 . The reality of navigating this “new normal” contributes to a high level of stress that is felt by many stroke survivors (SS) 4,5 …”
mentioning
confidence: 99%
“…1 Consequently, these patients may have to relearn how to perform activities of daily living while simultaneously trying to regain control of emotional and cognitive functions. 2,3 The reality of navigating this "new normal" contributes to a high level of stress that is felt by many stroke survivors (SS). 4,5 Stress disrupts the balance in a person's life and can be classified into 3 main categories: environmental, psychological, and biological.…”
BACKGROUND: Stroke survivors (SS) may experience alterations in physical and cognitive processes that increase stress and reduce well-being. Timely and accurate measurement of stress throughout the continuum of recovery is necessary to inform targeted interventions that will improve quality of life for this group. OBJECTIVE: The aim of this study was to describe the utilization of the Perceived Stress Scale (PSS) during recovery in SS. METHODS: A comprehensive literature search was conducted using CINAHL, PsycINFO, PubMed, and Scopus databases. Studies were included if they captured primary data collection using any version of the PSS at any time point in the poststroke recovery period and were published in English between 2011 and 2022. Systematic reviews and meta-analyses were excluded. Evidence was synthesized, and themes were discussed. RESULTS: Among 397 studies, a total of 13 met inclusion criteria. Of these, 8 were cross-sectional studies, 3 were longitudinal studies, 1 was a randomized controlled trial, and the remaining study was a prospective nonrandomized trial. The PSS-10 (n = 7, 54%) was the most used version of the instrument, followed by the PSS-14 (n = 3, 23%) and PSS-4 (n = 2, 15.4%), with the modified PSS-10 being used in only 1 (7.6%) study. The PSS surveys were administered at various time points, ranging from the first day of admission to 3, 6, 9, or 12 months after discharge. Perceived stress may continue to negatively influence SS's psychological and physical well-being throughout the chronic phase of recovery. CONCLUSIONS: Stress is a unique and individualized experience that influences recovery trajectories in SS, an experience often overlooked or marginalized by clinicians and healthcare providers. To help mobilize strategies to achieve long-term health and wellness goals, future studies should explore and tailor interventions to minimize the influence of stress, as identified by the PSS, on well-being and quality of life during poststroke recovery.
“…The most frequently used version of the scale was the PSS-10, found in 7 studies 2,19–24 . The PSS-14 was used less often, followed by the PSS-4 and the modified PSS 3,25–29 . Many studies (9) reported on the type and location of stroke (ie, descriptors including ischemic, hemorrhagic, left hemispheric, or right hemispheric stroke).…”
Section: Resultsmentioning
confidence: 99%
“…The PSS was collected at multiple time points across studies. In cross-sectional studies, collection varied from time of hospital admission to 7 days after stroke, a few months, or even 12 months or greater post stroke 2,3,19,20,25–28 . These studies reported moderate to high levels of PS, ranging from 5.0 for the PSS-4, 14.04 to 16.90 for the PSS-10, and 29.62 for the PSS-14 2,3,19,20,26,28 .…”
Section: Resultsmentioning
confidence: 99%
“…Although there are many additional contributing factors, most works found a correlation between scores in stroke severity and PS. 2,3,19,20,25,26 Worsening neurological deficits (National Institutes of Health Stroke Scale), poor scores on the Stroke Impact Scale, and greater impairment of cognitive function (cognitive FIM) and motor function (motor FIM) were associated with higher levels of PS. 2,3,19,20,25,26 PSS in Cross-sectional Studies.…”
Section: Resultsmentioning
confidence: 99%
“…Stroke is a leading cause of long-term disability, and almost 75% of survivors are left with some degree of physical disability 1 . Consequently, these patients may have to relearn how to perform activities of daily living while simultaneously trying to regain control of emotional and cognitive functions 2,3 . The reality of navigating this “new normal” contributes to a high level of stress that is felt by many stroke survivors (SS) 4,5 …”
mentioning
confidence: 99%
“…1 Consequently, these patients may have to relearn how to perform activities of daily living while simultaneously trying to regain control of emotional and cognitive functions. 2,3 The reality of navigating this "new normal" contributes to a high level of stress that is felt by many stroke survivors (SS). 4,5 Stress disrupts the balance in a person's life and can be classified into 3 main categories: environmental, psychological, and biological.…”
BACKGROUND: Stroke survivors (SS) may experience alterations in physical and cognitive processes that increase stress and reduce well-being. Timely and accurate measurement of stress throughout the continuum of recovery is necessary to inform targeted interventions that will improve quality of life for this group. OBJECTIVE: The aim of this study was to describe the utilization of the Perceived Stress Scale (PSS) during recovery in SS. METHODS: A comprehensive literature search was conducted using CINAHL, PsycINFO, PubMed, and Scopus databases. Studies were included if they captured primary data collection using any version of the PSS at any time point in the poststroke recovery period and were published in English between 2011 and 2022. Systematic reviews and meta-analyses were excluded. Evidence was synthesized, and themes were discussed. RESULTS: Among 397 studies, a total of 13 met inclusion criteria. Of these, 8 were cross-sectional studies, 3 were longitudinal studies, 1 was a randomized controlled trial, and the remaining study was a prospective nonrandomized trial. The PSS-10 (n = 7, 54%) was the most used version of the instrument, followed by the PSS-14 (n = 3, 23%) and PSS-4 (n = 2, 15.4%), with the modified PSS-10 being used in only 1 (7.6%) study. The PSS surveys were administered at various time points, ranging from the first day of admission to 3, 6, 9, or 12 months after discharge. Perceived stress may continue to negatively influence SS's psychological and physical well-being throughout the chronic phase of recovery. CONCLUSIONS: Stress is a unique and individualized experience that influences recovery trajectories in SS, an experience often overlooked or marginalized by clinicians and healthcare providers. To help mobilize strategies to achieve long-term health and wellness goals, future studies should explore and tailor interventions to minimize the influence of stress, as identified by the PSS, on well-being and quality of life during poststroke recovery.
Purpose:
Prior studies have shown that communication-related participation restrictions in patients with degenerative disease do not always match clinician judgment or objective indices of symptom severity. Although there is a growing body of literature documenting that discrepancies between patients with dementia and their care partners' perception of participation restrictions exist, it is not known how care partner perceptions of
communication
participation restrictions specifically match or diverge from the patients' experiences, which may inform the use of care partner proxy in the context of degenerative diseases.
Method:
Thirty-eight patients with progressive neurologic conditions (progressive supranuclear palsy, corticobasal syndrome, and primary progressive aphasia or apraxia of speech) and, in most instances, focal cognitive-communication disorders were included. The patients and their accompanying care partners independently completed the Communicative Participation Item Bank, short form, a 10-question survey about communication participation restrictions in different contexts. Care partners were instructed to complete the form with their perception of the patient's experience. The difference between patient and care partner total scores were calculated and analyzed relative to clinical and demographic variables of interest.
Results:
Care partner ratings modestly tracked with patient experience and objective indices of symptom severity but did not exactly match patient ratings. The presence of aphasia increased, but did not fully account for, the likelihood of a discrepancy between care partner and patient ratings.
Conclusion:
Although careful consideration should be given prior to using care-partner report as a proxy for patient experience, it is worthwhile to include care partner ratings as a means of supporting conversations about differing perceptions, guiding joint intervention planning, and monitoring care-partner perceptions of change along with the implementation of supported conversation strategies.
Purpose:
Supporting psychological well-being in persons with aphasia (PWA) can improve social and health outcomes; however, PWA and their care partners (CPs) are often not receiving mental health support. Previous research explores this from the perspective of health care professionals.
Aims:
The aim of this study was to examine knowledge, beliefs, and experiences related to mental health services directly from PWA and CPs.
Method:
The study included 11 PWA and 11 CPs. Participants completed a guided survey (virtual) with opportunities for elaboration related to the knowledge, beliefs, and experiences of mental health.
Results:
There was variability in personal preferences for referrals, types of coping strategies, and confidants for general thoughts and feelings and those specific to aphasia. PWA identified health care professionals as people to share thoughts and feelings, whereas CPs chose family and friends more often. Both CPs and PWA reported communication difficulty and finding a counselor as “sometimes” preventing access to services but cited fear and trust as “always” preventing access.
Conclusions:
Knowledge, beliefs, and experience with help-seeking and mental health services are personal and variable. Assessing barriers unique to living with aphasia, such as communication challenges and locating a suitable counselor, must also be considered within more complex and personal barriers of fear and trust that are consistently reported in the general public. Health professionals across the continuum of aphasia care need to understand the communication challenges of living with aphasia in tandem with understanding individual differences to personalize approaches to mental health services and help-seeking.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.