Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06109766 · ClinicalTrials.gov registry record · NA
Delivering Evidence-Based Parenting Services to Families in Child Welfare Using Telehealth
A NA study of Parenting and Parent-Child Relations, sponsored by University of Washington.
- Recruiting
- Registry status
- NA
- Development phase
- 357
- Enrollment target
- 1
- Study location
NCT06109766: Recruiting NA study of Parenting and Parent-Child Relations, sponsored by University of Washington.
NCT06109766 is a NA study of Parenting and Parent-Child Relations that is actively recruiting participants, run by University of Washington. The registered enrollment target is 357 participants, below the 643-participant average among 66 other Parenting trials with a reported enrollment target (44% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06109766, a NA study of Parenting and Parent-Child Relations, is actively recruiting participants, sponsored by University of Washington.
- RECRUITING
- Registry status
- NA
- Development phase
- 357 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this randomized controlled trial is to compare Promoting First Relationships - Home Visit (PFR-HV) to Promoting First Relationships - Telehealth (PFR-T) among parents of 6-12 month olds in the child welfare system. The main questions it aims to answer are: * Is PFR-T effective relative to PFR-HV and Usual Care with respect to observed parent sensitive and responsive care, parent knowledge of child social and emotional development, and child externalizing behavior? * Is PFR-T effective relative to PFR-HV and Usual Care with respect to child out-of-home placement in foster care relative to the control group? * How does PFR-T compare in a benefit-cost analysis to the cost-effectiveness relative to PFR-HV and Usual Care? * Are eligible families impacted by the lack of technology and Wi-Fi/cellular data to engage in PFR-T? * How does provider adherence and fidelity in delivery of PFR-T compare to adherence and fidelity of PFR-HV? What will participants be asked to do? 1. Participants will be asked to agree to randomization, resulting in their placement in one of three groups: PFR-HV, PFR-T, or the control group. 2. Participants will be asked to participate in three virtual research visits, over the course of approximately 12 months (families could be finished as early as 9 months, however in our experience, intervention sessions and research visits often need to be rescheduled, delaying completion of the study). The research visits take approximately 80 minutes, and families will be paid $75 for each visit they participate in. 3. During the research visit, the families will be asked to participate in videotaped research activities involving parent-child play and interaction. Parents will be asked to answer questions regarding their background, feelings, parenting opinions, and stress. 4. Families randomized to the PFR-HV intervention are asked to participate in a 10 week in home parenting program which includes videotaped caregiver-child interactions and f
Primary Outcome
Parent sensitivity is measured by the Nursing Child Assessment Teaching Scale (NCATS;Barnard 1994), a videotaped interaction to assess caregiver sensitivity, stimulation of the child, and emotional responsiveness during interaction.
Conditions Studied
Interventions
- BEHAVIORAL Promoting First Relationships
Study Locations (1)
Washington
- University of Washington - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 357 participants |
| Start Date | 2023-10-12 |
| Est. Completion | 2028-04-12 |
| Phase | NA |
What NCT06109766 shows while recruiting
NCT06109766 is an interventional study that assigns participants to a tested intervention. The registered 357 participants enrollment target is mid-sized for trials with a published cap, below the 643-participant average among 66 other Parenting trials with a reported enrollment target (44% lower).
The record links to 4 conditions, with Parenting appearing as the primary indexed condition, and to 1 intervention - of which Promoting First Relationships is the first listed.
NCT06109766 reports a single indexed study location in Washington.
Frequently Asked Questions
What is clinical trial NCT06109766 about?
NCT06109766 is a clinical study titled "Delivering Evidence-Based Parenting Services to Families in Child Welfare Using Telehealth". The goal of this randomized controlled trial is to compare Promoting First Relationships - Home Visit (PFR-HV) to Promoting First Relationships - Telehealth (PFR-T) among parents of 6-12 month olds in the child welfare system. The main questions it aims to answer are: * Is PFR-T effective relative ...
What is the current status of trial NCT06109766?
This trial is currently recruiting. It is a NA study. The enrollment target is 357 participants. The study started on 2023-10-12. Estimated completion is 2028-04-12.
What conditions does trial NCT06109766 study?
This clinical trial studies the following conditions: Parenting, Parent-Child Relations, Child Maltreatment, Child Behavior.
What interventions are being tested in trial NCT06109766?
The interventions under investigation include: Promoting First Relationships (BEHAVIORAL).
Who is sponsoring clinical trial NCT06109766?
This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06109766 being conducted?
This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Parenting
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06109766's enrollment target sits among peer trials
357 19th of 66 higher than 48 of 66 other Parenting trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Parenting trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Chicago Parent Program for Foster and Kinship Caregivers
RECRUITING · NA
-
Parent Intervention for Psychiatrically-Hospitalized Youth
RECRUITING · NA
-
Evaluation of the Parenting in the Moment Online Program for Forcibly Displaced Families
RECRUITING · NA
-
Pilot Trial of the RUBI Program for Autistic Adults
RECRUITING · NA
-
Intervening With Opioid-Dependent MothersMothers and Infants
RECRUITING · NA
-
I-InTERACT Preterm Parenting
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT06062888 · 357 participants · Phase 2
FFP In Traumatic BRAin INjury (FIT-BRAIN) Trial
- NCT06231342 · 357 participants · NA
Endotracheal Tube (ETT) 180: Stylet-loaded Endotracheal Tube Rotation Before Insertion
- NCT06533826 · 357 participants · Phase 2
TReatment of ADC-Refractory Breast CancEr With Dato-DXd or T-DXd: TRADE DXd
- NCT06679621 · 357 participants · NA
A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI