490 research outputs found
Using manipulated photographs to identify features of streetscapes that may encourage older adults to walk for transport
Experimental evidence of environmental features important for physical activity is challenging to procure in real world settings. The current study aimed to investigate the causal effects of environmental modifications on a photographed street\u27s appeal for older adults\u27 walking for transport. Secondly, we examined whether these effects differed according to gender, functional limitations, and current level of walking for transport. Thirdly, we examined whether different environmental modifications interacted with each other. Qualitative responses were also reported to gain deeper insight into the observed quantitative relationships. Two sets of 16 panoramic photographs of a streetscape were created, in which six environmental factors were manipulated (sidewalk evenness, traffic level, general upkeep, vegetation, separation from traffic, and benches). Sixty older adults sorted these photographs on appeal for walking for transport on a 7-point scale and reported qualitative information on the reasons for their rankings. Sidewalk evenness appeared to have the strongest influence on a street\u27s appeal for transport-related walking. The effect of sidewalk evenness was even stronger when the street\u27s overall upkeep was good and when traffic was absent. Absence of traffic, presence of vegetation, and separation from traffic also increased a street\u27s appeal for walking for transport. There were no moderating effects by gender or functional limitations. The presence of benches increased the streetscape\u27s appeal among participants who already walked for transport at least an hour/week. The protocols and methods used in the current study carry the potential to further our understanding of environment-PA relationships. Our findings indicated sidewalk evenness as the most important environmental factor influencing a street\u27s appeal for walking for transport among older adults. However, future research in larger samples and in real-life settings is needed to confirm current findings
The relationship between perceived promotion of autonomy/dependence and pain-related disability in older adults with chronic pain: the mediating role of self-reported physical functioning
Chronic pain is prevalent among older adults and is usually associated with high levels of functional disability. Social support for the promotion of functional autonomy and dependence has been associated with pain-related disability and self-reported physical functioning. Nevertheless, these relationships need further inquiry. Our aims were to investigate: (1) the relationship between perceived promotion of autonomy/dependence and pain-related disability and (2) the extent to which self-reported physical functioning mediated these relationships. 118 older adults (Mage = 81.0) with musculoskeletal chronic pain completed the Portuguese versions of the revised formal social support for Autonomy and Dependence in Pain Inventory, the pain severity and interference scales of the Brief Pain Inventory, and the physical functioning scale of the Medical Outcomes Study-Short-Form 36 v2. Higher levels of perceived promotion of autonomy were associated with lower pain-related disability; this relationship was partially mediated by self-reported physical functioning (B = -.767, p < .001 decreasing to B' = -.485, p < .01). Higher perceived promotion of dependence was associated with higher pain-related disability; this effect was also partially accounted for by self-reported physical functioning (B = .889, p < .01 decreasing to B' = .597, p < .05). These results highlight the importance of perceived promotion of autonomy and dependence for managing older adults' experience of chronic pain.info:eu-repo/semantics/acceptedVersio
Older adults’ preferences for formal social support of autonomy and dependence in pain: development and validation of a scale
Chronic pain among older adults is common and often disabling. Pain-related formal social support (e.g., provided by staff at day-care centres, nursing homes), and the extent to which it promotes functional autonomy or dependence, plays a significant role in the promotion of older adults’ ability to engage in their daily activities. Assessing older adults’ preferences for pain-related social support for functional autonomy or dependence could contribute to increase formal social support responsiveness to individuals’ needs. Therefore, this study aimed at developing and validating the Preferences for Formal Social Support of Autonomy and Dependence in pain Inventory (PFSSADI). One hundred and sixty five older adults with chronic musculoskeletal pain (Mage=79.1, 67.3% women), attending day-care centers, completed the PFSSADI, the revised Formal Social Support for Autonomy and Dependence in Pain Inventory, and a measure of desire for (in)dependence; the PFSSADI was filled out again 6 weeks later. Confirmatory factor analyses showed a structure of two correlated factors (r= .56): (a) Preferences for Autonomy Support (?=.99); and (b) Preferences for Dependence Support (?=.98). The scale showed good test-retest reliability, sensitivity and discriminant and concurrent validity; the higher the preferences for dependence support the higher the desire for dependence (r=.33) and the lower the desire for independence (r=-.41). The PFSSADI is an innovative tool, which may contribute to explore the role of pain-related social support responsiveness on the promotion of older adults’ functional autonomy when in pain.info:eu-repo/semantics/acceptedVersio
Older adults’ preferences for formal social support of autonomy and dependence in pain: development and validation of a scale
Chronic pain among older adults is common and often disabling. Pain-related formal social support (e.g., provided by staff at day-care centres, nursing homes), and the extent to which it promotes functional autonomy or dependence, plays a significant role in the promotion of older adults’ ability to engage in their daily activities. Assessing older adults’ preferences for pain-related social support for functional autonomy or dependence could contribute to increase formal social support responsiveness to individuals’ needs. Therefore, this study aimed at developing and validating the Preferences for Formal Social Support of Autonomy and Dependence in pain Inventory (PFSSADI). One hundred and sixty five older adults with chronic musculoskeletal pain (Mage=79.1, 67.3% women), attending day-care centers, completed the PFSSADI, the revised Formal Social Support for Autonomy and Dependence in Pain Inventory, and a measure of desire for (in)dependence; the PFSSADI was filled out again 6 weeks later. Confirmatory factor analyses showed a structure of two correlated factors (r= .56): (a) Preferences for Autonomy Support (?=.99); and (b) Preferences for Dependence Support (?=.98). The scale showed good test-retest reliability, sensitivity and discriminant and concurrent validity; the higher the preferences for dependence support the higher the desire for dependence (r=.33) and the lower the desire for independence (r=-.41). The PFSSADI is an innovative tool, which may contribute to explore the role of pain-related social support responsiveness on the promotion of older adults’ functional autonomy when in pain.info:eu-repo/semantics/acceptedVersio
The revised formal social support for autonomy and dependence in pain inventory (FSSADI_PAIN): confirmatory factor analysis and validity
ain among older adults is common and generally associated with high levels of functional disability. Despite its important role in elders' pain experiences, perceived (formal) social support (PSS) has shown inconsistent effects on their functional autonomy. This suggests a moderator role of 2 recently conceptualized functions of PSS: perceived promotion of dependence versus autonomy. The present study aimed at revising and further validating the Formal Social Support for Autonomy and Dependence in Pain Inventory (FSSADI_PAIN), which measures these 2 PSS functions among institutionalized elders in pain. Two hundred fifty older adults (mean age = 81.36 years, 75.2% women) completed the revised FSSADI_PAIN along with measures of physical functioning (ie, Medical Outcome Study Short Form-36) and informal PSS (ie, Social Support Scale of Medical Outcomes Study). Confirmatory factor analyses showed a good fit for a 2-factor structure: 1) perceived promotion of autonomy (n = 4 items; alpha = .89), and 2) perceived promotion of dependence (n = 4 items; alpha = .85). The revised FSSADI_PAIN showed good content, discriminant, and criterion-related validity; it discriminated the PSS of male and female older adults and also of elders with different levels of physical functioning. In conclusion, the revised FSSADI_PAIN is an innovative, valid, and reliable tool that allows us to assess 2 important functions of PSS, which may play a relevant role in the prevention and reduction of pain-related physical disability and functional dependence among institutionalized older adults. Perspective: This article presents a revised version of the FSSADI_PAIN that assesses elders' perceived promotion of functional autonomy/dependence as 2 independent functions of perceived social support. This measure may contribute to future research on the role of close interpersonal contexts on the promotion of active aging among elders with chronic pain.info:eu-repo/semantics/acceptedVersio
The perception, understanding and experience of flourishing in young people living with chronic pain: a Q-methodology study
Much research has adopted a deficits-based approach to chronic pain, neglecting the study of flourishing. Using a Q-methodological framework, this study sought to explore how individuals experience, understand and perceive flourishing in the context of young people living with chronic pain. Fifty-four individuals completed a Q-sorting task, indicating their level of agreement and disagreement with 52 statements. Q-analysis generated three factors that represented clear viewpoints of participants: ‘Pain is not a barrier to flourishing’, ‘Adapting to a new life’ and ‘Adopting a positive perspective’. Factors expressed the viewpoints that flexibility is key to enjoying life despite chronic pain, while resilience, management of stressors, acceptance and problem-solving may be required to flourish with chronic pain. Participants’ understanding of flourishing also focused on the appreciation and enjoyment of life and achievements. This study provides a useful contribution towards furthering our understanding of flourishing in young people living with chronic pain
Helping your partner with chronic pain: the importance of helping motivation, received social support, and its timeliness
Objective
Like all intentional acts, social support provision varies with respect to its underlying motives. Greater autonomous or volitional motives (e.g., enjoyment, full commitment) to help individuals with chronic pain (ICPs) are associated with greater well-being benefits for the latter, as indexed by improved satisfaction of their psychological needs for autonomy, competence, and relatedness. The present study investigates the processes explaining why partners’ autonomous or volitional helping motivation yields these benefits.
Methods
A total of 134 couples, where at least one partner had chronic pain, completed a 14-day diary. Partners reported on their daily helping motives, whereas ICPs reported on their daily received support, timing of help, need-based experiences, and pain.
Results
On days when partners provided help for volitional motives, ICPs indicated receiving more help, which partially accounted for the effect of autonomous helping motivation on ICP need-based experiences. Timing of help moderated the effects of daily received support on ICP need-based experiences.
Conclusions
Findings highlight the importance of ICPs of receiving support in general and the role of timing in particular, which especially matters when there is little support being received.info:eu-repo/semantics/acceptedVersio
Catastrophic thinking about pain: A critical appraisal highlighting the importance of the social context and balance
Numerous research studies have shown that endorsing a catastrophic interpretation about pain is associated with deleterious outcomes, such as higher levels of distress, pain intensity and disability for the person in pain. The fear-avoidance model has been found to be useful in explaining these associations by stressing that heightened feelings of distress and behaviour aimed at reducing or avoiding pain might be adaptive in an acute pain context but can become maladaptive when the pain becomes chronic. Pain is rarely a private event and the communal coping model underscores that the heightened pain expression in people endorsing catastrophic thoughts about pain could have a social, communicative function of eliciting empathic responses in others. However, these models are not all-encompassing. In particular, neither of the models takes into account the growing evidence indicating that catastrophic thinking in observers can also impact their emotional experience and behaviour in response to the other’s pain. Moreover, the context of multiple goals in which pain and pain behaviour occurs is largely ignored in both models. In this article we present an integrative perspective on catastrophic thinking that takes into account the social system and interplay between different goals people in pain and observers might pursue (e.g., school/work performance, leisure, social engagement). Specifically, this integrative perspective stresses the importance of considering the bidirectional influence between catastrophic thoughts in the person experiencing pain and observers. Furthermore, the importance of balance between pain-relief and other important goals as well as in the level of catastrophic thoughts in understanding the maladaptive influence of catastrophic thinking will be underlined. Clinical implications and future research directions of this integrated perspective are discussed
Coping with a dead end by relying on your own compass: A qualitative study on illness and treatment models in the context of fibromyalgia
Fibromyalgia lacks a coherent illness and treatment model, which includes a set of conceptual ideas shaping individuals’ perceptions and understandings of pain, its causing and maintaining factors, and management strategies. Developing personalized illness models that can guide treatment plans and alleviate feelings of uncertainty is of crucial importance. This study investigates how individuals with fibromyalgia develop a personal illness and treatment model while navigating the current healthcare system and explore their experiences during this process. Semi-structured interviews were conducted with 15 cis women with fibromyalgia, which were analyzed using reflexive thematic analysis. The analysis produced two themes, each including two subthemes. The first theme encompassed the difficulty of developing a comprehensive illness model due to the biomedical perspective of the healthcare system; the second theme described the importance of participants (re)gaining ownership and agency over their pain management, by constructing their own illness and treatment model. Most women in this study got stuck in the biomedical healthcare web not being provided with a clear illness and treatment model. Consequently, most women gained ownership of this process by developing their personal illness and treatment model (self-empowerment). Conversely, a few women felt powerless and paralyzed. This study underscores the importance of promoting patient empowerment in chronic pain management. Agency is undervalued in the treatment of fibromyalgia and warrants more thorough examination. Increasing knowledge about agency could enhance treatment effectiveness.info:eu-repo/semantics/acceptedVersio
The role of environment and AGN feedback in quenching local galaxies: Comparing cosmological hydrodynamical simulations to the SDSS
We present an analysis of the quenching of local observed and simulated
galaxies, including an investigation of the dependence of quiescence on both
intrinsic and environmental parameters. We apply an advanced machine learning
technique utilizing random forest classification to predict when galaxies are
star forming or quenched. We perform separate classification analyses for three
groups of galaxies: (a) central galaxies; (b) high-mass satellites (); and (c) low-mass satellites () for three cosmological hydrodynamical simulations (EAGLE,
Illustris, and IllustrisTNG), and observational data from the SDSS. The
simulation results are unanimous and unambiguous: quiescence in centrals and
high-mass satellites is best predicted by intrinsic parameters (specifically
central black hole mass), whilst it is best predicted by environmental
parameters (specifically halo mass) for low-mass satellites. In observations,
we find black hole mass to best predict quiescence for centrals and high mass
satellites, exactly as predicted by the simulations. However, local galaxy
over-density is found to be most predictive parameter for low-mass satellites.
Nonetheless, both simulations and observations do agree that it is environment
which quenches low mass satellites. We provide evidence which suggests that the
dominance of local over-density in classifying low mass systems may be due to
the high uncertainty in halo mass estimation from abundance matching, rather
than it being fundamentally a more predictive parameter. Finally, we establish
that the qualitative trends with environment predicted in simulations are
recoverable in the observation space. This has important implications for
future wide-field galaxy surveys.Comment: Accepted to MNRAS; 32 pages; 22 figure
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