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as well as assessment of problematic symptoms are conducted at the beginning, during, and at the end of treatment. Control subjects may include persons not being treated at the clinic or those on a wait-list for treatment. Because the experimenters cannot always decide who can receive treatment and who must remain wait-listed, randomization is impossible. Therefore many important differences between treated children and children not being treated at the clinic may exist and cannot be adequately controlled. Such practical limitations require much more caution in the interpretation of research findings than is the case with true experimental techniques, and direct cause-and-effect relationships cannot be inferred.

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SCIENTIFIC RESEARCH IN THE NATURALISTIC SETTING The present chapter has focused on the various experimental approaches for evaluating the ef cacy of therapeutic interventions and the methodological considerations necessary in conducting such investigations We have emphasized the importance of employing rigorous scienti c methodology in the quest for increasingly speci c cause-and-effect conclusions from internally valid investigations The types of studies that we have been describing are often called ef cacy studies and are characterized by the high degree of methodological rigor typical of clinical research conducted under controlled conditions.

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In particular, the World Humanity Action Trust advocates the use of a permitting approach (cf. Section 11.1.2) for both abstraction and discharges to water bodies (including aquifers), in which strict limits will be imposed on the duration, volume, and quality of all abstractions/ discharges, and in which the tariff structure is designed to encourage sustainable management practices (WHAT 2000). Design of appropriate tariff structures is a challenging activity. As for many other natural resources, the economic valuation of groundwater is not straightforward, due to the need to simultaneously evaluate the value of water in use, and the value of unused groundwater left in situ,

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Features of this kind of therapy research include the enrollment of carefully screened and diagnosed clients who are given a speci c number of therapy sessions in two or more randomly assigned comparison conditions administered by clinicians who have been thoroughly trained in each of the highly operationally de ned treatments that are described in detail in protocol manuals, supervised closely by project investigators, and checked for protocol adherence by independent assessors listening to tape recordings of the therapy sessions All of these features are of course incorporated to ensure the greatest degree of control over the experiment in order to reduce error variance and to provide the most unambiguous conclusions from the investigation.

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Among those who believe that therapy research is indeed capable of directly answering applied questions like Is this therapy effective or Which therapy is most effective , some have argued that the results of ef cacy investigations are not relevant to the applied setting because they lack external validity (cf Elliott, 1998) That is, the highly controlled and restrictive circumstances of ef cacy studies are so unlike what occurs in the real world of clinical intervention (eg, heterogeneous clients with frequently complex problems and comorbid conditions, absence of protocol manuals de ning how to intervene, absence of supervision, and variable length of treatment as determined by insurance policies or ability to self-pay) that the results of rigorous ef cacy experiments are unlikely to generalize to actual clinical practice.

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If one is focused on the scienti cally unanswerable questions about therapy effectiveness (rather than on causal relationships), then this criticism is well taken In the context of this criticism, a distinction is now often made between ef cacy investigations and what has been termed effectiveness research (eg, see Seligman, 1995) Effectiveness research refers to therapy studies that are conducted in real-world clinical settings In such research, there are often fewer or no restrictions on client participants (anyone who comes to a clinic can participate), and participating.

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I have tried the barcode control for BIRT , adding an EAN - 13 as a type and giving this barcode : 9002490100070, i get the following error : BarcodeItem (id = 73): ...
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