SKEZI
Paris, France
NCT Number: NCT07473466
This study is a randomized controlled trial nested in the "Le French Gut" e-cohort aiming to test the efficacy of 4 reminder strategies (emails and/or SMS with standard and/or institutional wording) in increasing participation of inactive volunteers.
This trial is led in collaboration between the "Le French Gut" project and SKEZI, a DeepTech start-up which markets the data collection solution (SKEZIA online platform) for the "Le French Gut" project and carries out the InnoPRO program, aimed at generating new knowledge in the field of e-cohorts.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Paris, France
The "Le French Gut" project (NCT05758961) is an ongoing online research cohort aiming to collect faecal samples and associated nutritional and clinical data to better understand the observed heterogeneity between gut microbiome of healthy subjects, its connections with the diet and lifestyle, but also changes in gut microbiota associated with diseases (diabetes, obesity, allergies, cancer, Parkinson, Alzheimer…). Le French Gut is initiated by MetaGenoPolis-INRAE, supported by INRAE with Prof. R. Benamouzig, (AP-HP) as principal investigator of the project.
When participants first register to participate in the cohort, they must complete a short "About You" ("A propos de vous") questionnaire before they can receive any study kits and be considered as active participants in the research. In October 2024, almost half of the ~43,000 individuals who have created an account never finish this first questionnaire needed to validate their participation in the cohort.
Purpose of the study This study will test which type of reminder works best for encouraging those inactive volunteers to return to the platform and complete the missing questionnaire.
How the study will be done
All eligible volunteers (i.e. people who registered on the online platform and provided a valid e mail address or mobile number but have not yet finished completing the "A propos de vous" questionnaire) will be randomly assigned to one of four groups:
All messages contain the same content (a link that takes the participant directly to the questionnaire). The study will last about one month after the last reminder is sent.
Questions the study will answer
Hypothesis Investigators hypothesized that the combined sequence (standard e mail → SMS → institutional e mail) will lead to a higher proportion of participants completing the questionnaire than any single channel reminder alone.
Why this matters Finding the most effective, low cost reminder strategy will help the French Gut team-and other online cohorts-keep more participants engaged, thereby improving the quantity and quality of the data that can be used for future health research. The results will be shared in a peer reviewed scientific article and could guide the design of future e cohort studies worldwide.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The same standard email is sent three times to participants, each email spaced 72 hours apart.
The same institutional email is sent three times to participants, each email spaced 72 hours apart.
The same SMS (brief text message) is sent three times to participants, each SMS spaced 72 hours apart.
Three reminders are sent to participants, each reminder spaced 72 hours apart: the first reminder is a standard email, the second reminder is a SMS, the third reminder is a institutional email.
Time frame: 30 days post-reminder
Proportion of participants who complete the "A propos de vous" questionnaire within 30 days after the last reminder, calculated as number of participants who fully completed the questionnaire divided by total number of participants included in the study (or arm)
Time frame: 30 days post-reminder
Time (in hours) between the date the last reminder was sent to a participant and the date of questionnaire completion
Time frame: 30 days post-reminder
Number of participants who logged into their account divided by total number of participants included in the study (or arm)
Time frame: 30 days post-reminder
Time (in hours) between the date the final reminder was sent to a participant and the date of their next login to the platform
Time frame: 30 days post-reminder
Number of opened emails divided by number of delivered emails
Time frame: 30 days post-reminder
Number of participants who clicked on the link in the email divided by number of opened emails
SKEZI
Industry
Le French Gut: Randomized-Controlled Trial to Evaluate Reminder Strategies (Emails and Text Messages) to Increase Participation in the Le French Gut E-cohort
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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