Association between interactive voice response adherence and subject retention in a randomized controlled trial
Abstract Introduction Interactive voice response (IVR) technology uses the telephone to collect patient reports. This study examined whether IVR adherence during a year-long clinical trial was related to subject retention in the trial. Methods As part of a randomized, double-blind, placebo-controlle...
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Veröffentlicht in: | Contemporary clinical trials 2012-07, Vol.33 (4), p.589-592 |
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description | Abstract Introduction Interactive voice response (IVR) technology uses the telephone to collect patient reports. This study examined whether IVR adherence during a year-long clinical trial was related to subject retention in the trial. Methods As part of a randomized, double-blind, placebo-controlled study of daily multivitamin supplementation for recurrent aphthous stomatitis, 160 study participants were asked to make 1 weekly IVR call for the one-year study duration. Results The 114 subjects who completed the study made 90.5% of their expected number of IVR calls, as compared to 55.7% of expected calls made by the 46 subjects who withdrew prematurely ( p < 0.001). Subjects who successfully completed the study were also more likely to initiate their IVR calls as compared to subjects who withdrew from the study ( p < 0.001). A multivariable model incorporating different adherence variables was able to successfully predict retention status of more than 80% of subjects. IVR adherence during the first few weeks of study participation was strongly predictive of subsequent retention and successful completion of this one-year study. Discussion Subjects who withdrew prematurely had more missing data than study completers, even after accounting for period of study participation, potentially introducing bias into IVR results. Sub-optimal adherence to weekly IVR might provide an early signal of subsequent premature withdrawal in clinical trials. IVR adherence could be used as a screening tool during a trial period, to identify subjects most likely to stay on long clinical trials. Conclusion IVR adherence may be useful in anticipating retention in long-term clinical studies. |
doi_str_mv | 10.1016/j.cct.2012.03.011 |
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This study examined whether IVR adherence during a year-long clinical trial was related to subject retention in the trial. Methods As part of a randomized, double-blind, placebo-controlled study of daily multivitamin supplementation for recurrent aphthous stomatitis, 160 study participants were asked to make 1 weekly IVR call for the one-year study duration. Results The 114 subjects who completed the study made 90.5% of their expected number of IVR calls, as compared to 55.7% of expected calls made by the 46 subjects who withdrew prematurely ( p < 0.001). Subjects who successfully completed the study were also more likely to initiate their IVR calls as compared to subjects who withdrew from the study ( p < 0.001). A multivariable model incorporating different adherence variables was able to successfully predict retention status of more than 80% of subjects. IVR adherence during the first few weeks of study participation was strongly predictive of subsequent retention and successful completion of this one-year study. Discussion Subjects who withdrew prematurely had more missing data than study completers, even after accounting for period of study participation, potentially introducing bias into IVR results. Sub-optimal adherence to weekly IVR might provide an early signal of subsequent premature withdrawal in clinical trials. IVR adherence could be used as a screening tool during a trial period, to identify subjects most likely to stay on long clinical trials. Conclusion IVR adherence may be useful in anticipating retention in long-term clinical studies.</description><identifier>ISSN: 1551-7144</identifier><identifier>EISSN: 1559-2030</identifier><identifier>DOI: 10.1016/j.cct.2012.03.011</identifier><identifier>PMID: 22484338</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cardiovascular ; Clinical research ; Compliance ; Data Collection - methods ; Dietary Supplements ; Hematology, Oncology and Palliative Medicine ; Humans ; Interactive voice response ; Interactive voice response systems ; IVR ; IVRS ; Multivariate Analysis ; Patient Compliance - statistics & numerical data ; Patient Dropouts - statistics & numerical data ; Randomized Controlled Trials as Topic - methods ; Reminder Systems ; Research Design ; Retention ; Stomatitis, Aphthous - drug therapy ; Telephone ; Vitamins - therapeutic use</subject><ispartof>Contemporary clinical trials, 2012-07, Vol.33 (4), p.589-592</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><rights>2012 Elsevier Inc. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-a4d2ee44be0c0efd1753eb4024047eefa71481c2e7b3b4d335ca1d10e4bc9bb23</citedby><cites>FETCH-LOGICAL-c506t-a4d2ee44be0c0efd1753eb4024047eefa71481c2e7b3b4d335ca1d10e4bc9bb23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1551714412000870$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22484338$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gatehouse, Christopher S</creatorcontrib><creatorcontrib>Tennen, Howard A</creatorcontrib><creatorcontrib>Feinn, Richard S</creatorcontrib><creatorcontrib>Abu-Hasaballah, Khamis S</creatorcontrib><creatorcontrib>Lalla, Rajesh V</creatorcontrib><title>Association between interactive voice response adherence and subject retention in a randomized controlled trial</title><title>Contemporary clinical trials</title><addtitle>Contemp Clin Trials</addtitle><description>Abstract Introduction Interactive voice response (IVR) technology uses the telephone to collect patient reports. This study examined whether IVR adherence during a year-long clinical trial was related to subject retention in the trial. Methods As part of a randomized, double-blind, placebo-controlled study of daily multivitamin supplementation for recurrent aphthous stomatitis, 160 study participants were asked to make 1 weekly IVR call for the one-year study duration. Results The 114 subjects who completed the study made 90.5% of their expected number of IVR calls, as compared to 55.7% of expected calls made by the 46 subjects who withdrew prematurely ( p < 0.001). Subjects who successfully completed the study were also more likely to initiate their IVR calls as compared to subjects who withdrew from the study ( p < 0.001). A multivariable model incorporating different adherence variables was able to successfully predict retention status of more than 80% of subjects. IVR adherence during the first few weeks of study participation was strongly predictive of subsequent retention and successful completion of this one-year study. Discussion Subjects who withdrew prematurely had more missing data than study completers, even after accounting for period of study participation, potentially introducing bias into IVR results. Sub-optimal adherence to weekly IVR might provide an early signal of subsequent premature withdrawal in clinical trials. IVR adherence could be used as a screening tool during a trial period, to identify subjects most likely to stay on long clinical trials. Conclusion IVR adherence may be useful in anticipating retention in long-term clinical studies.</description><subject>Cardiovascular</subject><subject>Clinical research</subject><subject>Compliance</subject><subject>Data Collection - methods</subject><subject>Dietary Supplements</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Interactive voice response</subject><subject>Interactive voice response systems</subject><subject>IVR</subject><subject>IVRS</subject><subject>Multivariate Analysis</subject><subject>Patient Compliance - statistics & numerical data</subject><subject>Patient Dropouts - statistics & numerical data</subject><subject>Randomized Controlled Trials as Topic - methods</subject><subject>Reminder Systems</subject><subject>Research Design</subject><subject>Retention</subject><subject>Stomatitis, Aphthous - drug therapy</subject><subject>Telephone</subject><subject>Vitamins - therapeutic use</subject><issn>1551-7144</issn><issn>1559-2030</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UstuFDEQHCEQecAHcEFz5DJDt-15REiRoggCUiQOwNnyo5d4mLUX27MofD2ebIiAAye33FXldlVX1QuEFgH711NrTG4ZIGuBt4D4qDrGrjtrGHB4fFdjM6AQR9VJShMA77u-e1odMSZGwfl4XIWLlIJxKrvga035B5Gvnc8UlcluT_U-OEN1pLQLPlGt7A1F8uVKeVunRU9kcmln8ncSzteqjqUXtu4n2doEn2OY51Lm6NT8rHqyUXOi5_fnafXl3dvPl--b649XHy4vrhvTQZ8bJSwjEkITGKCNxaHjpAUwAWIg2qjyqxENo0FzLSznnVFoEUhoc6Y146fV-UF3t-gtWVPGi2qWu-i2Kt7KoJz8u-Pdjfwa9pIXZYa8CLy6F4jh-0Ipy61LhuZZeQpLkiWAocd-hL5A8QA1MaQUafPwDMKK6-UkS1ByDUoClyWownn553wPjN_JFMCbA4CKS3tHUSbjVuOti8VyaYP7r_z5P2wzO--Mmr_RLaUpLNEX-yXKVDjy07op66IgA4BxAP4LdOm8gA</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Gatehouse, Christopher S</creator><creator>Tennen, Howard A</creator><creator>Feinn, Richard S</creator><creator>Abu-Hasaballah, Khamis S</creator><creator>Lalla, Rajesh V</creator><general>Elsevier Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120701</creationdate><title>Association between interactive voice response adherence and subject retention in a randomized controlled trial</title><author>Gatehouse, Christopher S ; Tennen, Howard A ; Feinn, Richard S ; Abu-Hasaballah, Khamis S ; Lalla, Rajesh V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-a4d2ee44be0c0efd1753eb4024047eefa71481c2e7b3b4d335ca1d10e4bc9bb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Cardiovascular</topic><topic>Clinical research</topic><topic>Compliance</topic><topic>Data Collection - methods</topic><topic>Dietary Supplements</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Interactive voice response</topic><topic>Interactive voice response systems</topic><topic>IVR</topic><topic>IVRS</topic><topic>Multivariate Analysis</topic><topic>Patient Compliance - statistics & numerical data</topic><topic>Patient Dropouts - statistics & numerical data</topic><topic>Randomized Controlled Trials as Topic - methods</topic><topic>Reminder Systems</topic><topic>Research Design</topic><topic>Retention</topic><topic>Stomatitis, Aphthous - drug therapy</topic><topic>Telephone</topic><topic>Vitamins - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gatehouse, Christopher S</creatorcontrib><creatorcontrib>Tennen, Howard A</creatorcontrib><creatorcontrib>Feinn, Richard S</creatorcontrib><creatorcontrib>Abu-Hasaballah, Khamis S</creatorcontrib><creatorcontrib>Lalla, Rajesh V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Contemporary clinical trials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gatehouse, Christopher S</au><au>Tennen, Howard A</au><au>Feinn, Richard S</au><au>Abu-Hasaballah, Khamis S</au><au>Lalla, Rajesh V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between interactive voice response adherence and subject retention in a randomized controlled trial</atitle><jtitle>Contemporary clinical trials</jtitle><addtitle>Contemp Clin Trials</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>33</volume><issue>4</issue><spage>589</spage><epage>592</epage><pages>589-592</pages><issn>1551-7144</issn><eissn>1559-2030</eissn><abstract>Abstract Introduction Interactive voice response (IVR) technology uses the telephone to collect patient reports. This study examined whether IVR adherence during a year-long clinical trial was related to subject retention in the trial. Methods As part of a randomized, double-blind, placebo-controlled study of daily multivitamin supplementation for recurrent aphthous stomatitis, 160 study participants were asked to make 1 weekly IVR call for the one-year study duration. Results The 114 subjects who completed the study made 90.5% of their expected number of IVR calls, as compared to 55.7% of expected calls made by the 46 subjects who withdrew prematurely ( p < 0.001). Subjects who successfully completed the study were also more likely to initiate their IVR calls as compared to subjects who withdrew from the study ( p < 0.001). A multivariable model incorporating different adherence variables was able to successfully predict retention status of more than 80% of subjects. IVR adherence during the first few weeks of study participation was strongly predictive of subsequent retention and successful completion of this one-year study. Discussion Subjects who withdrew prematurely had more missing data than study completers, even after accounting for period of study participation, potentially introducing bias into IVR results. Sub-optimal adherence to weekly IVR might provide an early signal of subsequent premature withdrawal in clinical trials. IVR adherence could be used as a screening tool during a trial period, to identify subjects most likely to stay on long clinical trials. Conclusion IVR adherence may be useful in anticipating retention in long-term clinical studies.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22484338</pmid><doi>10.1016/j.cct.2012.03.011</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cardiovascular Clinical research Compliance Data Collection - methods Dietary Supplements Hematology, Oncology and Palliative Medicine Humans Interactive voice response Interactive voice response systems IVR IVRS Multivariate Analysis Patient Compliance - statistics & numerical data Patient Dropouts - statistics & numerical data Randomized Controlled Trials as Topic - methods Reminder Systems Research Design Retention Stomatitis, Aphthous - drug therapy Telephone Vitamins - therapeutic use |
title | Association between interactive voice response adherence and subject retention in a randomized controlled trial |
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