Cargando…
Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial
Randomized double-blind placebo-controlled trials (RCTs) are regarded as the gold standard for clinical trials. While there are established standards to avoid unblinding, in RCTs using tetrahydrocannabinol (THC) containing cannabinoids, however, accidental unblinding and intentional self-unbinding m...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533554/ https://www.ncbi.nlm.nih.gov/pubmed/36213751 http://dx.doi.org/10.3389/fnins.2022.793703 |
_version_ | 1784802371806691328 |
---|---|
author | Müller-Vahl, Kirsten R. Jakubovski, Ewgeni Fremer, Carolin Lenz-Ziegenbein, Martina Großhennig, Anika Klages, Carolin Koch, Armin Haas, Martina Pisarenko, Anna |
author_facet | Müller-Vahl, Kirsten R. Jakubovski, Ewgeni Fremer, Carolin Lenz-Ziegenbein, Martina Großhennig, Anika Klages, Carolin Koch, Armin Haas, Martina Pisarenko, Anna |
author_sort | Müller-Vahl, Kirsten R. |
collection | PubMed |
description | Randomized double-blind placebo-controlled trials (RCTs) are regarded as the gold standard for clinical trials. While there are established standards to avoid unblinding, in RCTs using tetrahydrocannabinol (THC) containing cannabinoids, however, accidental unblinding and intentional self-unbinding must be considered as a particular issue, since THC tests are widely available. To investigate unblinding rates in an RCT using a THC-containing cannabinoid, we re-contacted 54 out of 97 participants of the CANNA-TICS trial who had participated in our study center in Hannover. Of the 54 participants, 53 could be reached. Of these, one participant (2%) stated that she had unblinded herself intentionally during the treatment phase, and another three patients (6%) reported intentional unblinding after the end of the treatment. Noteworthy, two patients provided discrepant information and denied self-unblinding during the interview, although during study/clinic visits they had reported having done so. Thus, based on all available information, three participants (6%) unblinded themselves intentionally during the treatment phase and another three (6%) after the end of the treatment. Accidental unblinding during the treatment phase was reported by 4/54 participants (7%) (during study visits). Since one participant reported both intentional self-unblinding (during the interview) and accidental unblinding (during a study visit), the total unblinding rate was 17% (n = 9). Of these, seven participants (13%) reported unblinding during the treatment phase. When asked in the interview whether they knew that self-unblinding would have been possible, only 34% (n = 18/53) of participants stated that they had been aware of this possibility. Thus, altogether 33% (n = 6/18) of those being informed about the possibility of self-unblinding did so and half of them (3/18, 17 %) during the treatment phase. It can be expected that in parallel to increasing knowledge of medicinal and recreational use of cannabinoids, more and more people will also be informed about the availability of THC tests. Hence, in future RCTs using THC-containing cannabinoids, researchers have to take the possibility of accidental and intentional unblinding into consideration, when designing the study. |
format | Online Article Text |
id | pubmed-9533554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95335542022-10-06 Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial Müller-Vahl, Kirsten R. Jakubovski, Ewgeni Fremer, Carolin Lenz-Ziegenbein, Martina Großhennig, Anika Klages, Carolin Koch, Armin Haas, Martina Pisarenko, Anna Front Neurosci Neuroscience Randomized double-blind placebo-controlled trials (RCTs) are regarded as the gold standard for clinical trials. While there are established standards to avoid unblinding, in RCTs using tetrahydrocannabinol (THC) containing cannabinoids, however, accidental unblinding and intentional self-unbinding must be considered as a particular issue, since THC tests are widely available. To investigate unblinding rates in an RCT using a THC-containing cannabinoid, we re-contacted 54 out of 97 participants of the CANNA-TICS trial who had participated in our study center in Hannover. Of the 54 participants, 53 could be reached. Of these, one participant (2%) stated that she had unblinded herself intentionally during the treatment phase, and another three patients (6%) reported intentional unblinding after the end of the treatment. Noteworthy, two patients provided discrepant information and denied self-unblinding during the interview, although during study/clinic visits they had reported having done so. Thus, based on all available information, three participants (6%) unblinded themselves intentionally during the treatment phase and another three (6%) after the end of the treatment. Accidental unblinding during the treatment phase was reported by 4/54 participants (7%) (during study visits). Since one participant reported both intentional self-unblinding (during the interview) and accidental unblinding (during a study visit), the total unblinding rate was 17% (n = 9). Of these, seven participants (13%) reported unblinding during the treatment phase. When asked in the interview whether they knew that self-unblinding would have been possible, only 34% (n = 18/53) of participants stated that they had been aware of this possibility. Thus, altogether 33% (n = 6/18) of those being informed about the possibility of self-unblinding did so and half of them (3/18, 17 %) during the treatment phase. It can be expected that in parallel to increasing knowledge of medicinal and recreational use of cannabinoids, more and more people will also be informed about the availability of THC tests. Hence, in future RCTs using THC-containing cannabinoids, researchers have to take the possibility of accidental and intentional unblinding into consideration, when designing the study. Frontiers Media S.A. 2022-09-21 /pmc/articles/PMC9533554/ /pubmed/36213751 http://dx.doi.org/10.3389/fnins.2022.793703 Text en Copyright © 2022 Müller-Vahl, Jakubovski, Fremer, Lenz-Ziegenbein, Großhennig, Klages, Koch, Haas and Pisarenko. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Müller-Vahl, Kirsten R. Jakubovski, Ewgeni Fremer, Carolin Lenz-Ziegenbein, Martina Großhennig, Anika Klages, Carolin Koch, Armin Haas, Martina Pisarenko, Anna Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial |
title | Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial |
title_full | Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial |
title_fullStr | Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial |
title_full_unstemmed | Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial |
title_short | Implications for blinding in clinical trials with THC-containing cannabinoids based on the CANNA-TICS trial |
title_sort | implications for blinding in clinical trials with thc-containing cannabinoids based on the canna-tics trial |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533554/ https://www.ncbi.nlm.nih.gov/pubmed/36213751 http://dx.doi.org/10.3389/fnins.2022.793703 |
work_keys_str_mv | AT mullervahlkirstenr implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT jakubovskiewgeni implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT fremercarolin implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT lenzziegenbeinmartina implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT großhenniganika implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT klagescarolin implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT kocharmin implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT haasmartina implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial AT pisarenkoanna implicationsforblindinginclinicaltrialswiththccontainingcannabinoidsbasedonthecannaticstrial |