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Recruitment and inclusion procedures as “pain killers” in clinical trials?

BACKGROUND: Recruitment and inclusion procedures in clinical trials are time critical. This holds particularly true for studies investigating patients with fluctuating symptom patterns, like those with chronic neck pain. In a feasibility study on neck pain, we found a clinically relevant decrease in...

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Autores principales: Nothnagel, H, Brown Menard, M, Kvarstein, G, Norheim, AJ, Weiss, T, Puta, C, Mist, SD, Musial, F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614587/
https://www.ncbi.nlm.nih.gov/pubmed/31308731
http://dx.doi.org/10.2147/JPR.S204259
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author Nothnagel, H
Brown Menard, M
Kvarstein, G
Norheim, AJ
Weiss, T
Puta, C
Mist, SD
Musial, F
author_facet Nothnagel, H
Brown Menard, M
Kvarstein, G
Norheim, AJ
Weiss, T
Puta, C
Mist, SD
Musial, F
author_sort Nothnagel, H
collection PubMed
description BACKGROUND: Recruitment and inclusion procedures in clinical trials are time critical. This holds particularly true for studies investigating patients with fluctuating symptom patterns, like those with chronic neck pain. In a feasibility study on neck pain, we found a clinically relevant decrease in pain ratings within the recruitment period. This paper analyses the phenomenon and gives recommendations for recruitment procedures in clinical trials on pain. METHODS: Changes in pain intensity scores of 44 chronic neck pain patients (6 males and 36 females; mean age: 45.3±13.2 years) between the first telephone contact and baseline assessment were analyzed. Inclusion criterion was a mean pain intensity of ≥40 on a 0–100 numerical rating scale during the last three months. Statistical analyses were performed using ANOVA and parametric/non-parametric correlation coefficients. RESULTS: Average pain intensity score decreased significantly from 60.3±13.3 at telephone interview to 38.1±21.7 at baseline assessment. This represents a relative change of 36.8%. A weak but significant negative correlation was found between number of days between assessments and pain rating differences. There was a positive correlation between change of pain intensity and the pain level at the first contact, indicating that the decreased pain ratings over time were also dependent on the initial pain rating. CONCLUSIONS: The clinically significant changes in pain intensity were weakly related to waiting time and moderately dependent on initial pain intensity, suggesting regression to the mean. The natural course of the disease and the Hawthorne effect are also discussed as contributing factors.
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spelling pubmed-66145872019-07-15 Recruitment and inclusion procedures as “pain killers” in clinical trials? Nothnagel, H Brown Menard, M Kvarstein, G Norheim, AJ Weiss, T Puta, C Mist, SD Musial, F J Pain Res Original Research BACKGROUND: Recruitment and inclusion procedures in clinical trials are time critical. This holds particularly true for studies investigating patients with fluctuating symptom patterns, like those with chronic neck pain. In a feasibility study on neck pain, we found a clinically relevant decrease in pain ratings within the recruitment period. This paper analyses the phenomenon and gives recommendations for recruitment procedures in clinical trials on pain. METHODS: Changes in pain intensity scores of 44 chronic neck pain patients (6 males and 36 females; mean age: 45.3±13.2 years) between the first telephone contact and baseline assessment were analyzed. Inclusion criterion was a mean pain intensity of ≥40 on a 0–100 numerical rating scale during the last three months. Statistical analyses were performed using ANOVA and parametric/non-parametric correlation coefficients. RESULTS: Average pain intensity score decreased significantly from 60.3±13.3 at telephone interview to 38.1±21.7 at baseline assessment. This represents a relative change of 36.8%. A weak but significant negative correlation was found between number of days between assessments and pain rating differences. There was a positive correlation between change of pain intensity and the pain level at the first contact, indicating that the decreased pain ratings over time were also dependent on the initial pain rating. CONCLUSIONS: The clinically significant changes in pain intensity were weakly related to waiting time and moderately dependent on initial pain intensity, suggesting regression to the mean. The natural course of the disease and the Hawthorne effect are also discussed as contributing factors. Dove 2019-07-03 /pmc/articles/PMC6614587/ /pubmed/31308731 http://dx.doi.org/10.2147/JPR.S204259 Text en © 2019 Nothnagel et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Nothnagel, H
Brown Menard, M
Kvarstein, G
Norheim, AJ
Weiss, T
Puta, C
Mist, SD
Musial, F
Recruitment and inclusion procedures as “pain killers” in clinical trials?
title Recruitment and inclusion procedures as “pain killers” in clinical trials?
title_full Recruitment and inclusion procedures as “pain killers” in clinical trials?
title_fullStr Recruitment and inclusion procedures as “pain killers” in clinical trials?
title_full_unstemmed Recruitment and inclusion procedures as “pain killers” in clinical trials?
title_short Recruitment and inclusion procedures as “pain killers” in clinical trials?
title_sort recruitment and inclusion procedures as “pain killers” in clinical trials?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614587/
https://www.ncbi.nlm.nih.gov/pubmed/31308731
http://dx.doi.org/10.2147/JPR.S204259
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