21 |
Sleep duration and moodSihra, Nirmal January 1996 (has links)
It is widely believed that sleep and mood are interrelated and that prolongation of sleep may have beneficial effects on subsequent mood and general well-being. In the present investigation, it is hypothesised that excess sleep is in fact, detrimental to mood and is associated with a 'Wornout Syndrome', characterised by feelings of fatigue and lethargy, that can persist for up to 5 hours. The studies to be presented here compare the differential effects of Sleep Extension and Sleep Restriction on mood in healthy adults. The experimental design required subjects to undergo one night of Sleep Extension [+2h] and, following an interval of one-week, one night of Sleep Reduction [-2h]. The conditions were counterbalanced. Subjective assessments were conducted hourly on mood states and sleepiness using an adapted Profile of Mood States Questionnaire and the Stanford Sleepiness Scale. Actometers were worn throughout the experimental days and nights. In the first study of 10 subjects results indicated that four subjects were adversely affected by oversleep. Study 2 investigated the effects of sleep duration on mood in 20 healthy adults. Personality factors were assessed using Cattell's 16PF Questionnaire. Subjects maintaining regular sleep schedules reported negative effects of oversleep on subsequent mood. Results indicated that certain personality types were predisposed to the 'Wornout Syndrome' following Sleep Extension. In Study 3, thirty-four subjects were selected on the basis of personality type. It was hypothesised that Introverts, Morning types, Emotionally Tenderminded and Low Impulsives would report symptoms characteristic of the 'Wornout Syndrome' following one night of Sleep Extension. This was confirmed by reports of increased fatigue, diminished vigor, and increased confusion following Sleep Extension. Oversleeping produced greater detrimental effects on mood than a comparable reduction in sleep duration. There are many similarities in symptomatology between the 'Wornout Syndrome' and Chronic Fatigue Syndrome (CFS), specifically, intense fatigue and impaired concentration. Interestingly, chronically fatigued patients often complain of sleep disturbance, and spend much of their time resting in bed. It was hypothesised that the 'Wornout Syndrome' may be a confounding factor in the symptomatology of CFS. As a clinical dimension, twelve subjects were investigated polysomnographically [six were CFS patients]. Findings indicated that CFS patients acquired sleep of longer duration than controls. In addition to excess nocturnal sleep, CFS patients were taking daytime naps. EEG data indicated that these individuals obtained twice the normal amount of slow wave sleep. CFS sufferers may be better advised to regulate their sleep habits and reduce their total sleep time to avoid the confounding effects of the 'Wornout Syndrome'.
|
22 |
Stigma and legitimation in chronic fatigue syndrome : the role of social locationBeaulieu, Marcia January 1997 (has links)
No description available.
|
23 |
Towards an ecosystemic understanding of Chronic Fatigue Syndrome (CFS)Skea, Charmaine Mary 31 January 2003 (has links)
Psychology / (M.A.(Clinical Psycholoy)
|
24 |
The Integrity of the circadian time-keeping system in chronic fatigue syndrome.Tooley, Gregory Allan, mikewood@deakin.edu.au January 2000 (has links)
Chronic Fatigue Syndrome (CFS) is a debilitating condition in which severe, ongoing fatigue is the most prominent of a complex of somatic, psychological and neuropsychological symptoms. The aetiology of CFS remains uncertain and, to date, efforts to distinguish a clear pathophysiological profile for the disorder have been unsuccessful. Current evidence suggests that, rather than being a discrete disease entity with a single cause, CFS is a clinical condition resulting from the interaction of a number of pathophysiological factors, including acute infections, stress and psychiatric disorder. Recently, there has been some interest in the proposition that disordered circadian time-keeping may contribute to the development and/or course of the illness. The rationale for the investigation of circadian factors in CFS is based on the fact that disorders known to be associated with circadian dysregulation, such as jet lag and shiftwork related syndromes have a high degree of symptomatological overlap with CFS. Also, the presence of circadian disturbance could account, in part, for other phenomenological aspects of CFS, including the high rates of comorbid affective disturbance, and the reports of low-level immune dyregulation among sufferers. While several recent studies have produced some evidence of chronobiological dysregulation in CFS patients, much work remains before conclusions can be drawn about the presence, nature and clinical significance of circadian disturbance in CFS. This thesis describes a series of studies that were designed to systematically investigate: 1. whether CFS is associated with a state of circadian dysregulation, and 2. whether circadian dysregulation contributes significantly to the symptomatology of CFS. The first of the 5 studies reported here compared the circadian patterns of sleep-activity of CFS sufferers with those of healthy controls. Results indicated that CFS patients' sleep-activity cycles were significantly phase delayed compared to controls, and that some aspects of their circadian profiles of sleep-activity were related to some measures of sleep-disturbance and well-being. Studies 2 and 3 investigated the relationship between rhythms of sleep-wake and core temperature in CFS patients and healthy controls. The major finding from these studies was that sleep-wake and core temperature rhythms appear to be less effectively synchronised. Further evidence was collected that suggested that there was a relationship between circadian parameters and symptom measures in the CFS group.
While this indicated that circadian dysregulation is linked in some way to the symptoms of CFS, assessment of the actual clinical significance of circadian disturbances required the use of a prospective methodology. The final two studies, therefore, report on a placebo-controlled trial of clinical interventions that were designed to restore circadian integrity to CFS patients, in order to see whether this would lead to a reduction in symptom number or severity. Results indicated that, although patients experienced improvements across a range of measures of symptoms and functional capacity, these were small in magnitude, of unlikely clinical significance, and no greater, in general, to improvements reported by patients who underwent placebo treatment. These results, along with those of the earlier studies, are discussed with respect to their implications regarding the presence and significance of circadian dysregulation. It is concluded that, while they provide evidence that CFS is associated with a degree of both internal and external circadian desynchrony, these findings suggest that circadian dysregulation is likely to be only a peripheral, contributor to the processes that generate and maintain the symptom complex. These findings are discussed with respect to how they contribute to our overall understanding of this multi-dimensional condition, and the implications they have for the continuing effort to investigate the causes and treatment of CFS.
|
25 |
From violation to reconstruction the process of self-renewal associated with chronic fatigue syndrome /Travers, Michele Kerry. January 2004 (has links)
Thesis (Ph. D.)--University of Sydney, 2004. / Title from title screen (viewed 5 May 2008). Includes questionnaires, interview guides, consent form, participant information sheet. Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy to the Dept. of Clinical Nursing, Faculty of Nursing. Includes bibliographical references. Also available in print form.
|
26 |
Towards an ecosystemic understanding of Chronic Fatigue Syndrome (CFS)Skea, Charmaine Mary 31 January 2003 (has links)
Psychology / (M.A.(Clinical Psycholoy)
|
27 |
Persoonlikheidskenmerke van chroniese moegheidsindroomlyersSmit, Susara Elena 11 February 2014 (has links)
M.A. (Psychology) / Please refer to full text to view abstract
|
28 |
A cognitive behavioural treatment programme for chronic fatigue syndrome sufferersFrazer, Melanie 07 September 2012 (has links)
D.Litt. et Phil. / The goal of this study was to determine the impact of cognitive behavioural therapy on people who meet the international diagnostic criteria for CFS, by specifically looking at symptoms and health behaviour. Whereas CFS was originally only studied from a medical perspective, recent years have seen an increased interest from psychologists. Initially the debate centered around whether CFS was a medical or psychiatric illness, but with the development of health psychology as a recognised field of its own, the focus shifted to the investigation of how medical and psychological factors work together to create the symptomatology of CFS. The approach adopted by the research team was that CFS was a biopsychosocial illness and that biological factors such as genetic predisposition, psychological factors such as cognitions and emotions and social factors such as the pressures of families and society work together to establish the health of a person. The study thus set out to gather information regarding all of these aspects in order to add to the current body of knowledge. As previous research efforts had been critisised regarding the validity of the diagnosis of the CFS patients included in their samples, an important challenge that was faced by the researcher was to establish that all the research group participants did meet with the diagnostic criteria. It also had to be ensured that their symptoms could not be accounted for by any other medical illness that was listed as an exclusion criteria for CFS. In order to achieve this patients who had not already had the necessary medical tests done, were requested to do so. The therapeutic intervention was based on cognitive behavioural principles which had been proven to be effective in the treatment of other illnesses that had a biological as well as psychological , aspect to it, for example anxiety, fibromyalgia and chronic pain. The aspects that were addressed had been found by previous researchers to be of great importance in a therapeutic intervention for CFS. These aspects included illness beliefs, information regarding CFS, locus of control and coping mechanisms, avoidance, activity levels, negative and dysfunctional thoughts, social support, lifestyle changes, stress management, sleep, exercise and personality factors. The specific techniques that were included in the intervention were self monitoring, monitoring and modifying of dysfunctional thoughts, goal setting, relaxation and systematic desensitisation. The research group consisted of 37 patients who met the internationally accepted diagnostic criteria for CFS. The control group was a contrast group of comparable size, which included only people who were free from psychological disorders and medical illnesses. The research group participated in a cognitive behavioural intervention, which was designed around the needs of each individual. They therapy was conducted at a community clinic at Rand Afrikaans University between February 1995 and October 1995. Pretests were completed upon commencement of the therapy and the posttests upon termination of the therapy. The control group completed their pre- and posttests at the average interval of the research group pre- and posttests. In order to make a multi-dimensional assessment of the impact of the cognitive behavioural intervention on CFS, various instruments were ulitised. The first instrument was a biographical questionnaire, which recorded the name, sex, age, income group, highest formal qualification, type of work, etcetera. The second questionnaire was an adapted version of the Support and Service Utilisation Schedule, which was employed to control for the other medical and therapeutic interventions that patients participated in, for example the medication taken, alternative medical practitioners visited and sources of support. The participants were asked to maintain their use of these services that they had been using for a long period and to not embark on any new therapies and treatments while they were partaking in the cognitive behavioural intervention.
|
29 |
The effectiveness of homoeopathic similimum treatment in chronic fatigue syndrome (CFS)Saul, Wayne January 2005 (has links)
Thesis (M.Tech.: Homoeopathy)-Dept. of Homoeopathy, Durban Institute of Technology, 2005
xxvii, 153 p. / Chronic fatigue syndrome (CFS) remains a medically unexplained syndrome, with differing aetiological models, case definitions and treatment recommendations (Ranjith, 2005:13). Sharpe & Wessely (1997:179) state that the current case definition for CFS has assumed acceptance as representing nothing more than a working definition of a clinical problem, pending further understanding. CFS has subsequently become the focus of much research and debate (Wessely, Hotopf & Sharpe, 1999:13). Notwithstanding, the definition in terms of diagnostic criteria is adequate in meeting the needs of research studies (Rutherford, 2003).
Anecdotal reports, espousing the effectiveness of homoeopathic treatment of CFS, points to the use of the similimum. (Bailey, 1995:189; De Schepper, 2001:6-7; Hardy, 2005:8-10). However, the limited research available on the subject suggests that more research needs to be conducted in this regard (Wessely, Hotopf & Sharpe, 1999:371; Walach, 2004:210-211).
This double-blind placebo-controlled study was conducted to determine the effectiveness of homoeopathic similimum treatment in chronic fatigue syndrome (CFS).
|
30 |
The psychological wellbeing of siblings of children with CFS/ME : a qualitative studyVelleman, Sophie January 2012 (has links)
Chronic Fatigue Syndrome or myalgic encephalopathy (CFS/ME) has a negative impact on a child and their parents. It is not known what the impact is for the siblings of children with CFS/ME. Nine siblings participated in semi-structured interviews. Siblings identified a number of negative impacts to their family and to themselves, as well as describing some protective family factors. These findings have implications for current practice in CFS/ME paediatric services.
|
Page generated in 0.0625 seconds