2011
DOI: 10.1007/s00520-011-1151-7
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A longitudinal study of changes in provider–patient interaction in treatment of localized prostate cancer

Abstract: Future research from both, the providers' and the patients' perspective, will have to clarify if we can interpret our results as change in the communication behaviour once the treatment decision for prostatectomy or hormonal therapy is made.

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Cited by 6 publications
(7 citation statements)
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“…urinary incontinence, LUTS or sexual dysfunction. Those symptoms and side‐effects might cause decisional regret about the RP and might lead to a more critical appraisal of physicians’ communication behaviour . Differences in the baseline scores between subscales continued over time, with information having the highest scores and devotion having the lowest scores.…”
Section: Discussionmentioning
confidence: 99%
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“…urinary incontinence, LUTS or sexual dysfunction. Those symptoms and side‐effects might cause decisional regret about the RP and might lead to a more critical appraisal of physicians’ communication behaviour . Differences in the baseline scores between subscales continued over time, with information having the highest scores and devotion having the lowest scores.…”
Section: Discussionmentioning
confidence: 99%
“…urinary incontinence, LUTS or sexual dysfunction. Those symptoms and side-effects might cause decisional regret about the RP and might lead to a more critical appraisal of physicians' communication behaviour [38]. Differences in the baseline scores between subscales continued According to communication theories, the most probable explanation for such associations would be the 'cognitive pathway' linking aspects of communication to patients' outcomes [35].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Most studies looking at how prostate cancer treatment decisions are made have focused on the process between the patient and the health care provider (Davison et al, 2009; Ernstmann et al, 2012; Underwood et al, 2010; Zikmund-Fisher et al, 2010). Fewer studies have looked at the decision process of patients and their partners (Boehmer & Clark, 2001; Schumm et al, 2010; Zeliadt et al, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…, and informed consent. For each patient, the initial information is documented (t 0 ); every 6 months thereafter, a follow-up documentation is then conducted, in which data are collected again regarding the general health of the participant, tumor stage, quality of life, doctor-patient interaction, and treatment satisfaction [31]. Four questions measure patient information about possible treatment options, rehabilitation options, self-help groups, and obtaining a second medical opinion.…”
Section: Research Questionmentioning
confidence: 99%