Does Educating Patients About the Early Palliative Care Study Increase Preferences for Outpatient Palliative Cancer Care? Findings From Project EMPOWER
Objectives: Randomized controlled trials, especially the Early Palliative Care Study (Temel et al., 2010), have shown that early outpatient palliative cancer care can improve quality of life for patients with advanced cancer or serious symptoms. However, fear and misconceptions drive avoidance of pa...
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Veröffentlicht in: | Health psychology 2017-06, Vol.36 (6), p.538-548 |
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description | Objectives: Randomized controlled trials, especially the Early Palliative Care Study (Temel et al., 2010), have shown that early outpatient palliative cancer care can improve quality of life for patients with advanced cancer or serious symptoms. However, fear and misconceptions drive avoidance of palliative care. Drawing from an empowerment perspective, we examined whether educating patients about evidence from the Early Palliative Care Study would increase preferences for palliative care. Method: A sample of 598 patients with prostate, breast, lung, colon/rectal, skin, and other cancer diagnoses completed an Internet-mediated experiment using a between-group prepost design. Intervention participants received a summary of the Early Palliative Care Study; controls received no intervention. Participants completed baseline and posttest assessments of preferences of palliative care. Analyses controlled for age, gender, education, cancer type, presence of metastases, time since diagnosis, and baseline preferences. Results: As hypothesized, the intervention had a favorable impact on participants' preferences for outpatient palliative cancer care relative to controls (d = 1.01, p < .001), while controlling for covariates. Intervention participants came to view palliative care as more efficacious (d = 0.79, p < .001) and less scary (d = 0.60, p < .001) and exhibited stronger behavioral intentions to utilize outpatient palliative care if referred (d = 0.60, p < .001). Findings were comparable in patients with metastatic disease, those with less education, and those experiencing financial strain. Conclusions: Educating patients about the Early Palliative Care Study increases preferences for early outpatient palliative care. This research has implications for future studies aimed at improving quality of life in cancer by increasing palliative care utilization. |
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Findings From Project EMPOWER</title><source>MEDLINE</source><source>EBSCOhost APA PsycARTICLES</source><source>Applied Social Sciences Index & Abstracts (ASSIA)</source><creator>Hoerger, Michael ; Perry, Laura M. ; Gramling, Robert ; Epstein, Ronald M. ; Duberstein, Paul R.</creator><contributor>Freedland, Kenneth E</contributor><creatorcontrib>Hoerger, Michael ; Perry, Laura M. ; Gramling, Robert ; Epstein, Ronald M. ; Duberstein, Paul R. ; Freedland, Kenneth E</creatorcontrib><description>Objectives: Randomized controlled trials, especially the Early Palliative Care Study (Temel et al., 2010), have shown that early outpatient palliative cancer care can improve quality of life for patients with advanced cancer or serious symptoms. However, fear and misconceptions drive avoidance of palliative care. Drawing from an empowerment perspective, we examined whether educating patients about evidence from the Early Palliative Care Study would increase preferences for palliative care. Method: A sample of 598 patients with prostate, breast, lung, colon/rectal, skin, and other cancer diagnoses completed an Internet-mediated experiment using a between-group prepost design. Intervention participants received a summary of the Early Palliative Care Study; controls received no intervention. Participants completed baseline and posttest assessments of preferences of palliative care. Analyses controlled for age, gender, education, cancer type, presence of metastases, time since diagnosis, and baseline preferences. Results: As hypothesized, the intervention had a favorable impact on participants' preferences for outpatient palliative cancer care relative to controls (d = 1.01, p < .001), while controlling for covariates. Intervention participants came to view palliative care as more efficacious (d = 0.79, p < .001) and less scary (d = 0.60, p < .001) and exhibited stronger behavioral intentions to utilize outpatient palliative care if referred (d = 0.60, p < .001). Findings were comparable in patients with metastatic disease, those with less education, and those experiencing financial strain. Conclusions: Educating patients about the Early Palliative Care Study increases preferences for early outpatient palliative care. This research has implications for future studies aimed at improving quality of life in cancer by increasing palliative care utilization.</description><identifier>ISSN: 0278-6133</identifier><identifier>EISSN: 1930-7810</identifier><identifier>DOI: 10.1037/hea0000489</identifier><identifier>PMID: 28277698</identifier><language>eng</language><publisher>United States: American Psychological Association</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Ambulatory Care - methods ; Avoidance behavior ; Breast cancer ; Cancer ; Client Education ; Clinical trials ; Early intervention ; Economic stress ; Education ; Empowerment ; Fear & phobias ; Female ; Health Care Utilization ; Health education ; Hospice care ; Human ; Humans ; Male ; Medical diagnosis ; Metastasis ; Middle Aged ; Misconceptions ; Neoplasms ; Neoplasms - psychology ; Outpatient Treatment ; Palliative Care ; Palliative Care - psychology ; Patient Education as Topic - methods ; Preferences ; Prostate ; Quality of Life ; Quality of Life - psychology ; Skin cancer</subject><ispartof>Health psychology, 2017-06, Vol.36 (6), p.538-548</ispartof><rights>2017 American Psychological Association</rights><rights>(c) 2017 APA, all rights reserved).</rights><rights>2017, American Psychological Association</rights><rights>Copyright American Psychological Association Jun 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a470t-2c7c262a28faf470384c00e2ccc387e1cbda9e8169c0fba5390a145b2a2759d23</citedby><orcidid>0000-0001-6882-0898</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904,30978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28277698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Freedland, Kenneth E</contributor><creatorcontrib>Hoerger, Michael</creatorcontrib><creatorcontrib>Perry, Laura M.</creatorcontrib><creatorcontrib>Gramling, Robert</creatorcontrib><creatorcontrib>Epstein, Ronald M.</creatorcontrib><creatorcontrib>Duberstein, Paul R.</creatorcontrib><title>Does Educating Patients About the Early Palliative Care Study Increase Preferences for Outpatient Palliative Cancer Care? Findings From Project EMPOWER</title><title>Health psychology</title><addtitle>Health Psychol</addtitle><description>Objectives: Randomized controlled trials, especially the Early Palliative Care Study (Temel et al., 2010), have shown that early outpatient palliative cancer care can improve quality of life for patients with advanced cancer or serious symptoms. However, fear and misconceptions drive avoidance of palliative care. Drawing from an empowerment perspective, we examined whether educating patients about evidence from the Early Palliative Care Study would increase preferences for palliative care. Method: A sample of 598 patients with prostate, breast, lung, colon/rectal, skin, and other cancer diagnoses completed an Internet-mediated experiment using a between-group prepost design. Intervention participants received a summary of the Early Palliative Care Study; controls received no intervention. Participants completed baseline and posttest assessments of preferences of palliative care. Analyses controlled for age, gender, education, cancer type, presence of metastases, time since diagnosis, and baseline preferences. Results: As hypothesized, the intervention had a favorable impact on participants' preferences for outpatient palliative cancer care relative to controls (d = 1.01, p < .001), while controlling for covariates. Intervention participants came to view palliative care as more efficacious (d = 0.79, p < .001) and less scary (d = 0.60, p < .001) and exhibited stronger behavioral intentions to utilize outpatient palliative care if referred (d = 0.60, p < .001). Findings were comparable in patients with metastatic disease, those with less education, and those experiencing financial strain. Conclusions: Educating patients about the Early Palliative Care Study increases preferences for early outpatient palliative care. This research has implications for future studies aimed at improving quality of life in cancer by increasing palliative care utilization.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Ambulatory Care - methods</subject><subject>Avoidance behavior</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Client Education</subject><subject>Clinical trials</subject><subject>Early intervention</subject><subject>Economic stress</subject><subject>Education</subject><subject>Empowerment</subject><subject>Fear & phobias</subject><subject>Female</subject><subject>Health Care Utilization</subject><subject>Health education</subject><subject>Hospice care</subject><subject>Human</subject><subject>Humans</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Misconceptions</subject><subject>Neoplasms</subject><subject>Neoplasms - psychology</subject><subject>Outpatient Treatment</subject><subject>Palliative Care</subject><subject>Palliative Care - psychology</subject><subject>Patient Education as Topic - methods</subject><subject>Preferences</subject><subject>Prostate</subject><subject>Quality of Life</subject><subject>Quality of Life - psychology</subject><subject>Skin cancer</subject><issn>0278-6133</issn><issn>1930-7810</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNp9ks2O0zAQgCMEYsvChQdAlrggUMA_SWxfFq1KCistasWPOFquM9mmSuNgOyv1SXhdpnRZWA74MpLn8-cZe7LsKaOvGRXyzQYsxVUofS-bMS1oLhWj97MZ5VLlFRPiJHsU4xYZrsvyYXbCFZey0mqW_XjnIZK6mZxN3XBFVhhgSJGcr_2USNoAqW3o95jo-w6T10DmNgD5nKZmTy4GF8BGIKsALQQYHNpaH8hySuNRdfckAuGX4C1ZdEODV0ayCH6HAr8Fl0j9cbX8Vn96nD1obR_hyU08zb4u6i_zD_nl8v3F_Pwyt4WkKedOOl5xy1VrW9wRqnCUAnfOCSWBuXVjNShWaUfbtS2FppYV5RpPyFI3XJxmZ0fvOK130DgsONjejKHb2bA33nbmbmboNubKX5uyKAotBQpe3AiC_z5BTGbXRQd9bwfwUzRMyarAPykO6PN_0K2fwoDtGaYZZ4JrNP6PUrIsKyV1hdTLI-WCjxEf_7ZkRs1hKsyfqUD42d9N3qK_xwCBV0fAjtaMce9sSJ3rIbop4Kemg8yIylSmFEr8BMzXwu4</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Hoerger, Michael</creator><creator>Perry, Laura M.</creator><creator>Gramling, Robert</creator><creator>Epstein, Ronald M.</creator><creator>Duberstein, Paul R.</creator><general>American Psychological Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7RZ</scope><scope>PSYQQ</scope><scope>7QJ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6882-0898</orcidid></search><sort><creationdate>20170601</creationdate><title>Does Educating Patients About the Early Palliative Care Study Increase Preferences for Outpatient Palliative Cancer Care? Findings From Project EMPOWER</title><author>Hoerger, Michael ; Perry, Laura M. ; Gramling, Robert ; Epstein, Ronald M. ; Duberstein, Paul R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a470t-2c7c262a28faf470384c00e2ccc387e1cbda9e8169c0fba5390a145b2a2759d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Ambulatory Care - methods</topic><topic>Avoidance behavior</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Client Education</topic><topic>Clinical trials</topic><topic>Early intervention</topic><topic>Economic stress</topic><topic>Education</topic><topic>Empowerment</topic><topic>Fear & phobias</topic><topic>Female</topic><topic>Health Care Utilization</topic><topic>Health education</topic><topic>Hospice care</topic><topic>Human</topic><topic>Humans</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Misconceptions</topic><topic>Neoplasms</topic><topic>Neoplasms - psychology</topic><topic>Outpatient Treatment</topic><topic>Palliative Care</topic><topic>Palliative Care - psychology</topic><topic>Patient Education as Topic - methods</topic><topic>Preferences</topic><topic>Prostate</topic><topic>Quality of Life</topic><topic>Quality of Life - psychology</topic><topic>Skin cancer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoerger, Michael</creatorcontrib><creatorcontrib>Perry, Laura M.</creatorcontrib><creatorcontrib>Gramling, Robert</creatorcontrib><creatorcontrib>Epstein, Ronald M.</creatorcontrib><creatorcontrib>Duberstein, Paul R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>APA PsycArticles®</collection><collection>ProQuest One Psychology</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Health psychology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoerger, Michael</au><au>Perry, Laura M.</au><au>Gramling, Robert</au><au>Epstein, Ronald M.</au><au>Duberstein, Paul R.</au><au>Freedland, Kenneth E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does Educating Patients About the Early Palliative Care Study Increase Preferences for Outpatient Palliative Cancer Care? Findings From Project EMPOWER</atitle><jtitle>Health psychology</jtitle><addtitle>Health Psychol</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>36</volume><issue>6</issue><spage>538</spage><epage>548</epage><pages>538-548</pages><issn>0278-6133</issn><eissn>1930-7810</eissn><abstract>Objectives: Randomized controlled trials, especially the Early Palliative Care Study (Temel et al., 2010), have shown that early outpatient palliative cancer care can improve quality of life for patients with advanced cancer or serious symptoms. However, fear and misconceptions drive avoidance of palliative care. Drawing from an empowerment perspective, we examined whether educating patients about evidence from the Early Palliative Care Study would increase preferences for palliative care. Method: A sample of 598 patients with prostate, breast, lung, colon/rectal, skin, and other cancer diagnoses completed an Internet-mediated experiment using a between-group prepost design. Intervention participants received a summary of the Early Palliative Care Study; controls received no intervention. Participants completed baseline and posttest assessments of preferences of palliative care. Analyses controlled for age, gender, education, cancer type, presence of metastases, time since diagnosis, and baseline preferences. Results: As hypothesized, the intervention had a favorable impact on participants' preferences for outpatient palliative cancer care relative to controls (d = 1.01, p < .001), while controlling for covariates. Intervention participants came to view palliative care as more efficacious (d = 0.79, p < .001) and less scary (d = 0.60, p < .001) and exhibited stronger behavioral intentions to utilize outpatient palliative care if referred (d = 0.60, p < .001). Findings were comparable in patients with metastatic disease, those with less education, and those experiencing financial strain. Conclusions: Educating patients about the Early Palliative Care Study increases preferences for early outpatient palliative care. This research has implications for future studies aimed at improving quality of life in cancer by increasing palliative care utilization.</abstract><cop>United States</cop><pub>American Psychological Association</pub><pmid>28277698</pmid><doi>10.1037/hea0000489</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-6882-0898</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Ambulatory Care - methods Avoidance behavior Breast cancer Cancer Client Education Clinical trials Early intervention Economic stress Education Empowerment Fear & phobias Female Health Care Utilization Health education Hospice care Human Humans Male Medical diagnosis Metastasis Middle Aged Misconceptions Neoplasms Neoplasms - psychology Outpatient Treatment Palliative Care Palliative Care - psychology Patient Education as Topic - methods Preferences Prostate Quality of Life Quality of Life - psychology Skin cancer |
title | Does Educating Patients About the Early Palliative Care Study Increase Preferences for Outpatient Palliative Cancer Care? Findings From Project EMPOWER |
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