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NCT06626750
Evaluating Stress Management Strategies Within the School Readiness Parenting Program
NA trial testing Summer Treatment Program for Pre-Kindergarteners and Kindergarteners in Parenting in 120 participants. Participants enrolled and being followed up; not accepting new ones.
29 May 2026
Quick facts
| Lead sponsor | Florida International University |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 120 |
| Start date | 7 February 2023 |
| Primary completion | 29 May 2026 |
| Estimated completion | 29 May 2026 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Summer Treatment Program for Pre-Kindergarteners and Kindergarteners
- School Readiness Parenting Program (SRPP)
- Cognitive Behavioral Therapy (CBT)
Conditions studied
- Parenting — all drugs for Parenting →
- Stress — all drugs for Stress →
- Disruptive Behavior Disorder — all drugs for Disruptive Behavior Disorder →
- Parent-Child Relations — all drugs for Parent-Child Relations →
Sponsor
Florida International University
Who can join
Adults 4 to 6, any sex, with Parenting or Stress. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this randomized study is to learn if adding three additional parent training sessions (focused on alleviating parental stress) to an already well-established treatment (School Readiness Parenting Program \[SRPP\]) in improving outcomes up to 6- and 12-months later for families of children with disruptive behavior disorders. The main questions it aims to answer are: The primary objective of this protocol is to evaluate the effects of three additional cognitive behavioral therapy (CBT) based parent training sessions to the SRPP to reduce parent stress and improve parent-child interactions. The secondary objective of this protocol is to evaluate the behavioral, emotional, and physical health-based functioning among young children with ADHD. Researchers will compare families who receive the SRPP alone to families who receive the SRPP + the three additional CBT focused sessions. Parents will be sent surveys to complete prior to the baseline assessment via REDCap (online). Parent and child participants will undergo 2 hours of baseline assessments evaluating behavioral, cognitive, and academic functioning as well as parent-child interactions. Parents will provide contact information for their child's teacher and the teacher will sent three surveys to complete online via REDCap.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06626750
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Other Florida International University trials
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06626750 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Florida International University
- Last refreshed: 20 October 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06626750.
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