Temptation

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The passage discusses temptation and how Jesus experienced and overcame temptation. It states that temptation comes through three fundamental human desires: bodily desires like food and comfort, human pride, and ambition or desire for power. Jesus was tempted in all of these ways but did not sin. He shows people how to overcome temptation through having strong trust in God, knowing one's self-worth, prayer, and avoiding occasions that could lead to wrongdoing.

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I composed this "One-page" solution to assist those individuals either suffering from fear of rejection or are trying to "rescued" loved ones from such a syndrome. As of this writing I have been married 28 years to a practicing clinical psychologist and have learned from many conversations that "forgiveness" is the key to a reconciled relationship with our heavenly Father. Forgiveness shall never be explained through reasoning but through the decision by the spirit (not the mind). It is not a process, one must simply "choose to forgive" on the basis that "God will reward us with peace that surpasses all understanding (reasoning)

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Trials with patient reported endpoints are reporting increased efficiencies when using electronic patient reported outcomes (ePRO), compared to paper diary data collection methods. To date, approximately 20% of all trials with patient reported endpoints are using ePRO solutions to collect efficacy data. As the adoption of electronic patient reported outcomes continues to increase, sponsors are finding new ways to justify this technology’s ROI, and identify the types of trials that are best suited to ePRO (versus paper). This article will describe how several market-leading sponsors have quantified the benefits of better data quality, with case examples from recent trials implemented by PHT Corporation (PHT). These analyses are provided with the intention to inform the clinical research community, and provide the frameworks for further ROI determinations.

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The importance of learning how patients feel and function when taking a new clinical therapy has been acknowledged by the FDA, EMA and other global regulatory authorities. Sponsors currently engaged in drug development programs appreciate and leverage the added value of patient-reported outcome (PRO) data. They no longer ask if PROs should be collected, but what phase to begin PRO collection. This issue of Insights is intended to identify the costs (delays and expenses) of collecting patient-reported outcomes on paper; and compare these against electronic PRO capture. The intention of this issue to provide clinical teams with industry data that can refute the presumption that paper methods are cheaper than ePRO.

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