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Search results for

"writing"

    Participant Engagement

    3 Tips to Avoid the Holiday Season Impacting Participant Compliance

    by Heather Ross December 13, 2023
    written by Heather Ross

    We often refer to participants as the heroes of research. Clinical trials and the medical advances made through research don’t happen without them. But here comes the holidays – will your study participant compliance waver during these busy times?

    Patient recruitment, retention, and compliance with study visits and procedures are central to the success of clinical trials. Schedules of events don’t provide much leeway, and holiday disruptions can become compliance headaches. Here are tips to get ahead of specific issues to keep your study and participants on track.

    Tip 1: Eat, Drink, and Be Compliant

    During the holidays, festive food provides tempting opportunities to overeat or indulge in foods that aren’t part of our normal diets. Also, holiday festivities, travel, and gatherings can throw study participants off their normal schedule. This can potentially disrupt study participant compliance with items such as:

    • Dietary restrictions or low-calorie diets
    • Exercise schedules
    • Alcohol intake limitations
    • Caffeine intake limitations
    • When to take the study drug
    • How to take the study drug (i.e., on an empty stomach)

    Provide reminders to participants of study parameters so they can still stay on track with study compliance. Also, you might be able to reschedule a site visit within the visit window if you see that, for example, the site visit occurs the morning after the participant’s gala family soiree.

    Tip 2: Help Clear Holiday Disruptions

    Holidays can easily unravel a family routine. Your participant may have family members visiting. Or, just having the children home from school all day for a couple of weeks could limit your participant’s availability.

    Here are 2 options:

    • Can your site arrange on-site childcare for visit days?
    • Can your site provide flexible scheduling with evening or weekend visits?

    Sometimes participant compliance rests on overcoming a temporary obstacle.

    Tip 3: Work With the Sponsor or CRO to Accommodate Snowbirds

    Snowbirds are northerners who move to a warmer southern locale in the winter. If you live in an area where participants are likely to migrate based on the weather (hot or cold), it’s important to assess this prior to enrollment. However, sometimes participants forget to disclose this, or their plans change.

    If a potential participant is perfect for a difficult-to-recruit study and is a snowbird, or you’re trying to keep an enrolled patient in a study, there may be some options to help.

    Does the study offer remote options that would work for the times the participant would be out of town? If in-person procedures are needed for these visits, consider working with the sponsor/CRO to see if there is another study site in the destination area and if they would allow (and the site would be willing) to perform the interim study visits.

    Final Thoughts

    If your participants see the lengths you are going through to ensure compliance over the holidays, it will likely reinforce to them the importance of not skipping visits.

    Participant compliance and retention are challenges even in the best of times, and communication can go a long way. Making sure your participant feels appreciated is a key to compliance and retention throughout the study. A surprising number of participants say they’ve never been thanked for taking part in studies, and the holidays are a great time to do this.

    December 13, 2023 0 comments
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  • Translation of Clinical Trial Materials

    Clinical Trial Translation: Precision Is Key

    by Erica Manning May 9, 2023
    by Erica Manning May 9, 2023

    Accurate clinical trial translation services are key to the overall success of a study. Each participant needs to receive the same information in their native language to ensure consistent study messaging across all languages and accuracy to the protocol. I’ve compiled key translation best practices …

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  • Clinical Trial Business InsightsParticipant Engagement

    Clinical Study Startup and Execution: Hidden Causes Behind Big Delays

    by Dan McDonald October 21, 2022
    by Dan McDonald October 21, 2022

    Before you plan your next study, please read this first. Planning and conducting a clinical trial presents numerous challenges, and we find that many sponsors and CROs repeatedly miss important areas when planning their studies. These planning gaps result in: Delayed clinical study startup Missing …

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  • Ancillary Clinical Trial Supplies and EquipmentClinical Trial Business InsightsClinical Trial Materials Development and PrintingParticipant EngagementTranslation of Clinical Trial Materials

    Clinical Trial Efficiencies: The Power of a Single Workstream

    by Dan McDonald August 18, 2022
    by Dan McDonald August 18, 2022

    The management time needed to corral many different elements during a trial is immense. In the buildup to a research study, clinical operations teams often focus on items such as study startup, site initiation and activation, supply chain, monitoring, data management, and safety. And there …

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  • Translation of Clinical Trial Materials

    Machine Translation: OK for Your Clinical Trial Materials?

    by Sian Lukaszewicz February 15, 2022
    by Sian Lukaszewicz February 15, 2022

    The number of global trials grows every year, with study teams reaching out to increasingly diverse patient populations. These broader populations bring a growing variety of languages, cultures, and experiences – all of which need to be considered when recruiting or interacting with clinical trial …

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  • Clinical Trial Business Insights

    DPHARM Conference Hits Year 11: Driven by COVID, it Delivers its Proof of Concept

    by Dan McDonald October 5, 2021
    by Dan McDonald October 5, 2021

    Like many conferences in the COVID era, DPHARM, the annual conference based in Boston and focused on disruptive innovations in clinical trials, moved from in-person to a virtual setting this week, due to local spikes of the Delta variant. To date, I’ve largely avoided these …

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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Writing Patient-Friendly Clinical Trial Materials: 3 Steps to Simplify Language & Increase Readability

    by William McEwen June 24, 2021
    by William McEwen June 24, 2021

    Introduction The clinical trials industry relies heavily on print and digital materials for patient recruitment and retention. To be effective, these materials must connect with the audience. There are many ways to make this connection, from writing clinical trial materials to designing them. One common …

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  • Clinical Trial Business Insights

    Our Best Blog Posts of 2019

    by William McEwen January 15, 2020
    by William McEwen January 15, 2020

    Happy 2020 from Imperial Clinical Research Services! In welcoming the New Year, it’s a good time to reflect on the highlights of 2019 and look ahead to new opportunities. Imperial proudly provides clinical research-oriented blogs and ebooks provided by our diverse and knowledgeable subject matter …

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  • Clinical Trial Materials Development and Printing

    Writing for Clinical Trial Patients, Sites, and Providers

    by William McEwen November 15, 2019
    by William McEwen November 15, 2019

    At Imperial, we generate millions of words for the clinical trial industry every year. Millions? Something like that, anyway. We specialize in writing recruitment, retention, and professional materials for clinical studies and we’ve just released our latest ebook called 6 Essentials When Writing Content for …

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  • Clinical Trial Business InsightsClinical Trial Materials Development and PrintingParticipant Engagement

    Plain Language – It’s for everyone

    by William McEwen October 24, 2019
    by William McEwen October 24, 2019

    According to the Institute of Medicine, there is a significant disparity between the health information people receive and actually understand. Even those in the health care industry can become vulnerable to not comprehending health information. When experiencing poor health or worry and stress about an …

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