85 research outputs found
Time-Series Photometry of Globular Clusters: M62 (NGC 6266), the Most RR Lyrae-Rich Globular Cluster in the Galaxy?
We present new time-series CCD photometry, in the B and V bands, for the
moderately metal-rich ([Fe/H] ~ -1.3) Galactic globular cluster (GC) M62 (NGC
6266). The present dataset is the largest obtained so far for this cluster, and
consists of 168 images per filter, obtained with the Warsaw 1.3m telescope at
the Las Campanas Observatory (LCO) and the 1.3m telescope of the Cerro Tololo
Inter-American Observatory (CTIO), in two separate runs over the time span of
three months. The procedure adopted to detect the variable stars was the
optimal image subtraction method (ISIS v2.2), as implemented by Alard. The
photometry was performed using both ISIS and DAOPHOT/ALLFRAME. We have
identified 245 variable stars in the cluster fields that have been analyzed so
far, of which 179 are new discoveries. Of these variables, 133 are fundamental
mode RR Lyrae stars (RRab), 76 are first overtone (RRc) pulsators, 4 are type
II Cepheids, 25 are long-period variables (LPV), 1 is an eclipsing binary, and
6 are not yet well classified. Such a large number of RR Lyrae stars places M62
among the top two most RR Lyrae-rich (in the sense of total number of RR Lyrae
stars present) GCs known in the Galaxy, second only to M3 (NGC 5272) with a
total of 230 known RR Lyrae stars. Since this study covers most but not all of
the cluster area, it is not unlikely that M62 is in fact the most RR Lyrae-rich
GC in the Galaxy. In like vein, we were also able to detect the largest sample
of LPV's known in a Galactic GC. We analyze a variety of Oosterhoff type
indicators for the cluster, and conclude that M62 is an Oosterhoff type I
system. This is in good agreement with the moderately high metallicity of the
cluster, in spite of its predominantly blue horizontal branch morphology --
which is more typical of Oosterhoff type II systems. We thus conclude that
metallicity plays a key role in defining Oosterhoff type. [abridged]Comment: 22 pages, 14 figures (emulateapj format). AJ, in pres
The Globular Cluster Omega Centauri and the Oosterhoff Dichotomy
CCD observations obtained by the OGLE team for 128 RR Lyrae variables in
Omega Cen have been analysed. The P-L and P-A plots indicate that, in addition
to fundamental (RRab) and first overtone (RRc) pulsators, the Omega Cen RR
Lyrae population seems to include second overtone (RRe) and possibly third
overtone pulsators. The mean periods derived for the RRab and RRc stars are
typical values for an Oosterhoff type II (OoII) cluster. Nevertheless, the P-A
plot plot also shows that some of the RR Lyrae variables have `Oosterhoff type
I' (OoI) characteristics. Relative luminosities derived for the RRc variables
from Fourier coefficients correlate with the observed apparent magnitudes.
Masses for the RRc stars have been calculated from Fourier coefficients. A
comparison of the derived masses for RRc stars in the four OoII clusters Omega
Cen, M15, M55 and M68 indicates that the masses of the RRc stars in M15 and M68
are almost 0.2 solar masses greater than those in the other two. Since M15 and
M68 have a high frequency of RRd stars among their first overtone pulsators,
while none have been identified in Omega Cen or M55, this suggests that the
double-mode pulsation phenomenon may be associated with mass. Among the RRc
variables in Omega Cen, the OoII variables have lower derived masses and higher
luminosities than the OoI variables. An application of the period-density law
to pairs of OoI and OoII RRab stars selected according to their position in the
P-A plot also indicates that the OoII variables in general have lower masses
and higher luminosities. These findings support the hypothesis that RR Lyrae
variables in OoII systems are evolved HB stars that spend their ZAHB phase on
the blue side of the instability strip.Comment: 52 pages, 10 figures, to appear in the AJ (November 2000
Effectiveness and cost-effectiveness of an internet intervention for family caregivers of people with dementia: design of a randomized controlled trial
<p>Abstract</p> <p>Background</p> <p>The number of people with dementia is rising rapidly as a consequence of the greying of the world population. There is an urgent need to develop cost effective approaches that meet the needs of people with dementia and their family caregivers. Depression, feelings of burden and caregiver stress are common and serious health problems in these family caregivers. Different kinds of interventions are developed to prevent or reduce the negative psychological consequences of caregiving. The use of internet interventions is still very limited, although they may be a cost effective way to support family caregivers in an earlier stage and diminish their psychological distress in the short and longer run.</p> <p>Methods/design</p> <p>A pragmatic randomized controlled trial is designed to evaluate the effectiveness and cost-effectiveness of ‘Mastery over Dementia’, an internet intervention for caregivers of people with dementia. The intervention aims at prevention and decrease of psychological distress, in particular depressive symptoms. The experimental condition consists of an internet course with 8 sessions and a booster session over a maximum period of 6 months guided by a psychologist. Caregivers in the comparison condition receive a minimal intervention. In addition to a pre and post measurement, an intermediate measurement will be conducted. In addition, there will be two follow-up measurements 3 and 6 months after post-treatment in the experimental group only. To study the effectiveness of the intervention, depressive symptoms are used as the primary outcome, whereas symptoms of anxiety, role overload and caregiver perceived stress are used as secondary outcomes. To study which caregivers profit most of the internet intervention, several variables that may modify the impact of the intervention are taken into account. Regarding the cost-effectiveness, an economic evaluation will be conducted from a societal perspective.</p> <p>Discussion</p> <p>This study will provide evidence about the effectiveness and cost-effectiveness of an internet intervention for caregivers. If both can be shown, this might set the stage for the development of a range of internet interventions in the field of caregiving for people with dementia. This is even more important because future generations of caregivers will be more familiar with the use of internet.</p> <p>Trial registration</p> <p>NTR-2051/RCT-DDB</p
Implementation of Internet-based preventive interventions for depression and anxiety: role of support? The design of a randomized controlled trial
<p>Abstract</p> <p>Background</p> <p>Internet-based self-help is an effective preventive intervention for highly prevalent disorders, such as depression and anxiety. It is not clear, however, whether it is necessary to offer these interventions with professional support or if they work without any guidance. In case support is necessary, it is not clear which level of support is needed. This study examines whether an internet-based self-help intervention with a coach is more effective than the same intervention without a coach in terms of clinical outcomes, drop-out and economic costs. Moreover, we will investigate which level of support by a coach is more effective compared to other levels of support.</p> <p>Methods</p> <p>In this randomized controlled trial, a total of 500 subjects (18 year and older) from the general population with mild to moderate depression and/or anxiety will be assigned to one of five conditions: (1) web-based problem solving through the internet (self-examination therapy) without a coach; (2) the same as 1, but with the possibility to ask help from a coach on the initiative of the respondent (on demand, by email); (3) the same as 1, but with weekly scheduled contacts initiated by a coach (once per week, by email); (4) weekly scheduled contacts initiated by a coach, but no web-based intervention; (5) information only (through the internet). The interventions will consist of five weekly lessons. Primary outcome measures are symptoms of depression and anxiety. Secondary outcome measures are drop-out from the intervention, quality of life, and economic costs. Other secondary outcome measures that may predict outcome are also studied, e.g. client satisfaction and problem-solving skills. Measures are taken at baseline (pre-test), directly after the intervention (post-test, five weeks after baseline), 3 months later, and 12 months later. Analysis will be conducted on the intention-to-treat sample.</p> <p>Discussion</p> <p>This study aims to provide more insight into the clinical effectiveness, differences in drop-out rate and costs between interventions with and without support, and in particular different levels of support. This is important to know in relation to the dissemination of internet-based self-help interventions.</p> <p>Trial Registration</p> <p>Nederlands Trial Register (NTR): TC1355</p
Two cases of "cannabis acute psychosis" following the administration of oral cannabis
BACKGROUND: Cannabis is the most commonly used illegal drug and its therapeutic aspects have a growing interest. Short-term psychotic reactions have been described but not clearly with synthetic oral THC, especially in occasional users. CASE PRESENTATIONS: We report two cases of healthy subjects who were occasional but regular cannabis users without psychiatric history who developed transient psychotic symptoms (depersonalization, paranoid feelings and derealisation) following oral administration of cannabis. In contrast to most other case reports where circumstances and blood concentrations are unknown, the two cases reported here happened under experimental conditions with all subjects negative for cannabis, opiates, amphetamines, cocaine, benzodiazepines and alcohol, and therefore the ingested dose, the time-events of effects on behavior and performance as well as the cannabinoid blood levels were documented. CONCLUSION: While the oral route of administration achieves only limited blood concentrations, significant psychotic reactions may occur
Effectiveness of behavioural graded activity compared with physiotherapy treatment in chronic neck pain: design of a randomised clinical trial [ISRCTN88733332]
BACKGROUND: Chronic neck pain is a common complaint in the Netherlands with a point prevalence of 14.3%. Patients with chronic neck pain are often referred to a physiotherapist and, although many treatments are available, it remains unclear which type of treatment is to be preferred. The objective of this article is to present the design of a randomised clinical trial, Ephysion, which examines the clinical and cost effectiveness of behavioural graded activity compared with a physiotherapy treatment for patients with chronic non-specific neck pain. METHODS: Eligible patients with non-specific neck pain persisting longer than 3 months will be randomly allocated to either the behavioural graded activity programme or to the physiotherapy treatment. The graded activity programme is based on an operant approach, which uses a time-contingent method to increase the patient's activity level. This treatment is compared with physiotherapy treatment using a pain-contingent method. Primary treatment outcome is the patient's global perceived effect concerning recovery from the complaint. Global perceived effect on daily functioning is also explored as primary outcome to establish the impact of treatment on daily activity. Direct and indirect costs will also be assessed. Secondary outcomes include the patient's main complaints, pain intensity, medical consumption, functional status, quality of life, and psychological variables. Recruitment of patients will take place up to the end of the year 2004 and follow-up measurement will continue until end 2005
The effectiveness and cost-evaluation of manual therapy and physical therapy in patients with sub-acute and chronic non specific neck pain. Rationale and design of a Randomized Controlled Trial (RCT)
Contains fulltext :
88910.pdf (publisher's version ) (Open Access)BACKGROUND: Manual Therapy applied to patients with non specific neck pain has been investigated several times. In the Netherlands, manual therapy as applied according to the Utrecht School of Manual Therapy (MTU) has not been the subject of a randomized controlled trial. MTU differs in diagnoses and treatment from other forms of manual therapy. METHODS/DESIGN: This is a single blind randomized controlled trial in patients with sub-acute and chronic non specific neck pain. Patients with neck complaints existing for two weeks (minimum) till one year (maximum) will participate in the trial. 180 participants will be recruited in thirteen primary health care centres in the Netherlands.The experimental group will be treated with MTU during a six week period. The control group will be treated with physical therapy (standard care, mainly active exercise therapy), also for a period of six weeks.Primary outcomes are Global Perceived Effect (GPE) and functional status (Neck Disability Index (NDI-DV)). Secondary outcomes are neck pain (Numeric Rating Scale (NRS)), Eurocol, costs and quality of life (SF36). DISCUSSION: This paper presents details on the rationale of MTU, design, methods and operational aspects of the trial. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT00713843
Where’s WALY? : A proof of concept study of the ‘wellbeing adjusted life year’ using secondary analysis of cross-sectional survey data
Background
The Quality-Adjusted Life Year (QALY) is a measure that combines life extension and health improvement in a single score, reflecting preferences around different types of health gain. It can therefore be used to inform decision-making around allocation of health care resources to mutually exclusive options that would produce qualitatively different health benefits. A number of quality-of-life instruments can be used to calculate QALYs. The EQ-5D is one of the most commonly used, and is the preferred option for submissions to NICE (https://www.nice.org.uk/process/pmg9/). However, it has limitations that might make it unsuitable for use in areas such as public and mental health where interventions may aim to improve well-being. One alternative to the QALY is a Wellbeing-Adjusted Life Year. In this study we explore the need for a Wellbeing-Adjusted Life Year measure by examining the extent to which a measure of wellbeing (the Warwick-Edinburgh Mental Well-being Scale) maps onto the EQ-5D-3L.
Methods
Secondary analyses were conducted on data from the Coventry Household Survey in which 7469 participants completed the EQ-5D-3L, Warwick-Edinburgh Mental Well-being Scale, and a measure of self-rated health. Data were analysed using descriptive statistics, Pearson’s and Spearman’s correlations, linear regression, and receiver operating characteristic curves.
Results
Approximately 75 % of participants scored the maximum on the EQ-5D-3L. Those with maximum EQ-5D-3L scores reported a wide range of levels of mental wellbeing. Both the Warwick-Edinburgh Mental Well-being Scale and the EQ-5D-3L were able to detect differences between those with higher and lower levels of self-reported health. Linear regression indicated that scores on the Warwick-Edinburgh Mental Well-being Scale and the EQ-5D-3L were weakly, positively correlated (with R2 being 0.104 for the index and 0.141 for the visual analogue scale).
Conclusion
The Warwick-Edinburgh Mental Well-being Scale maps onto the EQ-5D-3L to only a limited extent. Levels of mental wellbeing varied greatly amongst participants who had the maximum score on the EQ-5D-3L. To evaluate the relative effectiveness of interventions that impact on mental wellbeing, a new measure – a Wellbeing Adjusted Life Year – is needed
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