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Recruiting to Clinical Trials on the Telephone – a randomized controlled trial
BACKGROUND: Informed consent is an essential element of clinical research. Obtaining consent, however, may be challenging. The use of the telephone for giving information and obtaining consent may be practical but little formal research has been done. METHODS: We examined the use of the telephone fo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117558/ https://www.ncbi.nlm.nih.gov/pubmed/27871308 http://dx.doi.org/10.1186/s13063-016-1680-y |
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author | Foss, Kim Thestrup Kjærgaard, Jesper Stensballe, Lone Graff Greisen, Gorm |
author_facet | Foss, Kim Thestrup Kjærgaard, Jesper Stensballe, Lone Graff Greisen, Gorm |
author_sort | Foss, Kim Thestrup |
collection | PubMed |
description | BACKGROUND: Informed consent is an essential element of clinical research. Obtaining consent, however, may be challenging. The use of the telephone for giving information and obtaining consent may be practical but little formal research has been done. METHODS: We examined the use of the telephone for the purpose of informing expectant mothers about The Danish Calmette Study; a randomized clinical trial assessing neonatal Bacille Calmette-Guérin vaccination. Expectant mothers received an invitation letter with a Participant Information Sheet about The Danish Calmette Study, the present trial, and a Consent Form. Two to 4 weeks later we contacted the mothers to discuss potential participation in the present trial. At this initial telephone contact, and after consent from the mothers, we randomized expectant mothers to receive the verbal information about The Danish Calmette Study by telephone, or at a face-to-face consultation. The primary outcome was a communication score, consisting of comprehension of information about The Danish Calmette Study and satisfaction with the information process. The outcome was measured using a questionnaire 2 days after the information was provided, and 2.5 months after the birth of the child. RESULTS: The communication score obtained 2 days after information was given was significantly reduced in the telephone group, effect size −0.74 (95% confidence interval (CI), −1.11 to −0.36). The effect sizes of the subscores were −0.87 (95% CI, −1.25 to −0.49) for satisfaction and −0.22 (95% CI, −0.58 to 0.14) for comprehension. The effect sizes were slightly reduced when assessed 2.5 months after the birth. CONCLUSION: The communication score was reduced in the telephone group. This was due to a reduction in satisfaction, while no difference in the comprehension could be found in comparison to the control group. This may be ethically acceptable as both groups had high satisfaction scores. TRIAL REGISTRATION: ClinicalTrials.gov, registered on 5 October 2015 with trial registration number NCT02570061. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1680-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5117558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51175582016-11-28 Recruiting to Clinical Trials on the Telephone – a randomized controlled trial Foss, Kim Thestrup Kjærgaard, Jesper Stensballe, Lone Graff Greisen, Gorm Trials Research BACKGROUND: Informed consent is an essential element of clinical research. Obtaining consent, however, may be challenging. The use of the telephone for giving information and obtaining consent may be practical but little formal research has been done. METHODS: We examined the use of the telephone for the purpose of informing expectant mothers about The Danish Calmette Study; a randomized clinical trial assessing neonatal Bacille Calmette-Guérin vaccination. Expectant mothers received an invitation letter with a Participant Information Sheet about The Danish Calmette Study, the present trial, and a Consent Form. Two to 4 weeks later we contacted the mothers to discuss potential participation in the present trial. At this initial telephone contact, and after consent from the mothers, we randomized expectant mothers to receive the verbal information about The Danish Calmette Study by telephone, or at a face-to-face consultation. The primary outcome was a communication score, consisting of comprehension of information about The Danish Calmette Study and satisfaction with the information process. The outcome was measured using a questionnaire 2 days after the information was provided, and 2.5 months after the birth of the child. RESULTS: The communication score obtained 2 days after information was given was significantly reduced in the telephone group, effect size −0.74 (95% confidence interval (CI), −1.11 to −0.36). The effect sizes of the subscores were −0.87 (95% CI, −1.25 to −0.49) for satisfaction and −0.22 (95% CI, −0.58 to 0.14) for comprehension. The effect sizes were slightly reduced when assessed 2.5 months after the birth. CONCLUSION: The communication score was reduced in the telephone group. This was due to a reduction in satisfaction, while no difference in the comprehension could be found in comparison to the control group. This may be ethically acceptable as both groups had high satisfaction scores. TRIAL REGISTRATION: ClinicalTrials.gov, registered on 5 October 2015 with trial registration number NCT02570061. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1680-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-21 /pmc/articles/PMC5117558/ /pubmed/27871308 http://dx.doi.org/10.1186/s13063-016-1680-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Foss, Kim Thestrup Kjærgaard, Jesper Stensballe, Lone Graff Greisen, Gorm Recruiting to Clinical Trials on the Telephone – a randomized controlled trial |
title | Recruiting to Clinical Trials on the Telephone – a randomized controlled trial |
title_full | Recruiting to Clinical Trials on the Telephone – a randomized controlled trial |
title_fullStr | Recruiting to Clinical Trials on the Telephone – a randomized controlled trial |
title_full_unstemmed | Recruiting to Clinical Trials on the Telephone – a randomized controlled trial |
title_short | Recruiting to Clinical Trials on the Telephone – a randomized controlled trial |
title_sort | recruiting to clinical trials on the telephone – a randomized controlled trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117558/ https://www.ncbi.nlm.nih.gov/pubmed/27871308 http://dx.doi.org/10.1186/s13063-016-1680-y |
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