Evaluating the Psychometric Properties of Three Clinical Trial Outcome Measures for Rett Syndrome

  • STATUS
    Recruiting
Updated on 30 June 2022
Online studies

Summary

Evaluating the Psychometric Properties of Three Clinical Trial Outcome Measures for Rett Syndrome: The purpose of this research study is to document the psychometric properties of three non-invasive, clinic-friendly, and quantifiable outcome measures reflecting pathologically- and clinically-relevant symptoms of Rett Syndrome (RTT). Despite several ongoing or pending clinical trials for pharmaceutical interventions in RTT, there are currently no agreed-upon outcome measures sufficiently validated for use in the RTT patient population. We have identified three potential non-invasive measures that reflect clinical features of RTT and that have preliminary evidence of feasibility. The next step is to document the reliability and validity of these measures in clinical populations. We also plan to pilot an ambulatory measure of skin temperature that has been used in other clinical populations, as a means to evaluate peripheral temperature fluctuations and diurnal patterns. 
 
The study consists of two components: a virtual research visit with our research team via Zoom and two, in-home collection periods using wearable technology. The virtual research visit will last around 1 hour, and we will ask parents/guardians of participants questions about their child's health, behavior, and mood. After the virtual visit, we will also send additional questionnaires via email for families to complete on their own time. 
 
The two, in-home collection periods will last for 14 days, 4-6 weeks apart. Research staff will send a sleep watch, and 3 temperature sensors to the family's home. During these collection periods, we will ask families to have their child wear a sleep watch (looks like a Fitbit) for 14 days. This sleep watch will record the participant's activity when they are asleep and awake. We will ask families to fill out a sleep diary for their child during this time too. Families will repeat this process 4-6 weeks later. 
 
In addition to the sleep watch, we will ask participants to wear 3, small temperature sensors on their feet and abdomen. These temperature sensors will be taped the participant's feet and abdomen using hypoallergenic tape. We will also families to leave the temperature sensors on their child's body for 7 days. Families will repeat this process 4-6 weeks later as well. 

Description

- Clinically or genetically-diagnosed Rett syndrome, MECP2 duplication syndrome, CDKL5 syndrome, FOXG1 syndrome, or a pathogenic mutation of MECP2, CDKL5, or FOXG1 with intellectual/developmental delay without a diagnosis of Rett syndrome. 
- Non-verbal or minimally verbal. 
- All ages. 

Details
Condition Rett syndrome- congenital variety, Rett syndrome- atypical, Rett Syndrome, Cdkl5-related, Rett syndrome- preserved speech variety
Clinical Study IdentifierTX257658
Last Modified on30 June 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Clinically or genetically-diagnosed Rett syndrome, MECP2 duplication syndrome, CDKL5 syndrome, FOXG1 syndrome, or a pathogenic mutation of MECP2, CDKL5, or FOXG1 with intellectual/developmental delay without a diagnosis of Rett syndrome
Non-verbal or minimally verbal
All ages
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note