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Clinical Research

    Patient EngagementPatient Recruitment and Retention

    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 comment
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  • Business InsightsPatient EngagementStudy Site Management

    Asking Why Bolsters Clinical Trial Communication and Success

    by Hope Cullen October 24, 2023
    by Hope Cullen October 24, 2023

    Explore the importance of providing context for decisions in clinical trials to foster improved communication, trust, and success. “Why” seems to be at the center of what we do. Kids are always asking, “Why, Mom?” Lean Fundamentals teaches us the 5 Whys, and Simon Sinek…

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  • Life-Science EventsPatient Recruitment and Retention

    Clinical Trials Summit Brings Stakeholders to the Table

    by Alejandro Serricchio October 18, 2023
    by Alejandro Serricchio October 18, 2023

    The 2023 Global Site Solutions Summit successfully brought clinical trial sites, sponsors, CROs, and vendors together to express concerns and develop comprehensive solutions. Like most of you, I’ve attended many conferences related to the clinical trial industry. Some would say too many! But anyone expecting…

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  • Business InsightsClinical Trial Writing and DesignPatient Recruitment and Retention

    Clinical Research Phases and the Path to Drug Approval

    by Sian Lukaszewicz August 8, 2023
    by Sian Lukaszewicz August 8, 2023

    Getting a drug from the bench to the bedside takes around 10-15 years and around 6-7 of those years are spent in clinical trials. While it’s difficult to determine the exact amount, the cost of drug development appears to range from less than $1 billion to…

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  • Patient EngagementPatient Recruitment and RetentionStudy Site Management

    Clinical Trial Enrollment Timelines: Hidden Causes Behind Big Delays

    by Dan McDonald December 22, 2022
    by Dan McDonald December 22, 2022

    This is the second in my three-part series revealing hidden causes behind delays in clinical studies. The first part is here. This installment explores strategies to meet clinical trial enrollment goals. Tell me when your first patient was enrolled, and I will tell you the…

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  • Patient Recruitment and RetentionSite Materials & Logistics

    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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  • Business InsightsPatient Recruitment and Retention

    Artificial Intelligence for Clinical Trials: Move Ahead, or Halt?

    by Erica Manning July 26, 2022
    by Erica Manning July 26, 2022

    This blog was featured on Clinical Trial AI Weekly. For centuries, science fiction writers have toyed with the endless possibilities of artificial intelligence (AI). And now we’re living the future those writers celebrated and also feared. How might AI apply in the realities of our…

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  • Business InsightsClinical Trial Writing and Design

    Top Clinical Trial Branding Strategies

    by Vaughn X. Anthony February 12, 2019
    by Vaughn X. Anthony February 12, 2019

    In this series, we have discussed elements of branding, including what branding is, different creative elements, and how to work well with others. Now let’s look at strategy. These are the big-picture things to keep in mind throughout the process — from developing your clinical…

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  • Business InsightsClinical Trial Writing and Design

    Content Meets Design: Bringing Your Clinical Trial Materials to Life

    by Vaughn X. Anthony August 26, 2018
    by Vaughn X. Anthony August 26, 2018

    The creative process is serious business, and for this blog post, I’d like to focus on two areas: clinical study content and design.  Creating clinical study materials, such as a website or a poster to recruit patients, contain these two key elements. Each element is…

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  • Ancillary Trial Supplies and EquipmentBusiness InsightsLife-Science EventsPatient Recruitment and Retention

    Bridging Research and Health Care: If We Don’t Do it, Someone Else Will

    by Dan McDonald May 21, 2018
    by Dan McDonald May 21, 2018

    I recently had the honor and privilege of representing Imperial at the inaugural Bridging Clinical Research and Clinical Health Care conference in National Harbor, Maryland. It was interesting and worthwhile. The conference brought together heavy hitters and important voices, including the FDA and advocates from…

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Popular Posts

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  • Site Materials & Logistics (50)
  • Study Site Management (22)
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Imperial Clinical Research Services Blog

Imperial is a global leader in clinical trial solutions and support, specializing in study and site print materials, ancillary trial supplies and equipment, clinical trial translation management, and clinical trial patient engagement.

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