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Behavioral Intervention

CareMeds Intervention for Acute Lymphoblastic Leukemia

N/A
Recruiting
Led By Elizabeth Bouchard, PhD
Research Sponsored by Roswell Park Cancer Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 3 years
Awards & highlights

Study Summary

"This trial will test if the CareMeds program is practical and well-received by a larger group of 100 people in different locations in Buffalo, NY, and Atlanta, GA."

Who is the study for?
This trial is for parents of children aged 3-9 with acute lymphoblastic leukemia (ALL), who are fluent in English or Spanish, understand the study's nature, and have signed consent. The child must be on home-based oral anti-cancer medication like 6-MP.Check my eligibility
What is being tested?
The CareMeds Intervention is being tested against usual care to see if it helps improve how well parents manage their child’s medication for ALL. This larger study involves multiple sites and aims to evaluate its acceptability and feasibility.See study design
What are the potential side effects?
Since this trial focuses on behavioral intervention rather than a medical treatment, there may not be direct side effects like those associated with drugs; however, participation could impact family routines or stress levels.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 3 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 3 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Feasibility of the CareMeds 3 sessions
Secondary outcome measures
Behavioral Parenting skills
Oral Chemotherapy adherence

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: CareMeds InterventionExperimental Treatment1 Intervention
Participants complete the CareMeds parent training sessions during weeks 2, 3 and 4.
Group II: Usual CareActive Control2 Interventions
Usual care consists of medical consultations and supportive care, The usual care group will serve as a delayed intervention/wait list group for which 3 parent training sessions will be offered during weeks 13 through 15.

Find a Location

Who is running the clinical trial?

National Cancer Institute (NCI)NIH
13,669 Previous Clinical Trials
40,926,301 Total Patients Enrolled
Roswell Park Cancer InstituteLead Sponsor
402 Previous Clinical Trials
30,707 Total Patients Enrolled
Elizabeth Bouchard, PhDPrincipal InvestigatorRoswell Park Comprehensive Cancer Center
1 Previous Clinical Trials
79 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the total number of participants currently under investigation in this clinical study?

"Yes, according to details on clinicaltrials.gov, this research study is actively seeking participants. The trial was initially listed on April 1st, 2024 and last revised on March 5th, 2024. Researchers aim to recruit a total of 100 patients from one designated site."

Answered by AI

Is the registration process currently ongoing for this clinical trial?

"The information provided on clinicaltrials.gov confirms that this research study is currently seeking eligible participants. Initially shared on April 1, 2024, the trial's most recent update was noted on March 5, 2024."

Answered by AI

Are individuals older than 60 years being included in the recruitment for this study?

"To be eligible for this research study, individuals between 3 and 9 years old are sought after. Notably, there are a total of 301 investigations focused on the pediatric population under 18 years old and another 298 trials catering to participants over the age of 65."

Answered by AI
~67 spots leftby Apr 2027