Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03403153 · ClinicalTrials.gov registry record · NA

Parenting Strength At Home- Parents Pilot

A NA study of Parenting Behaviors and PTSD Symptoms, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
91
Enrollment target
3
Study locations

NCT03403153: Completed NA study of Parenting Behaviors and PTSD Symptoms, sponsored by VA Office of Research and Development.

NCT03403153 is a NA study of Parenting Behaviors and PTSD Symptoms that has completed, run by VA Office of Research and Development. The registered enrollment target is 91 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03403153, a NA study of Parenting Behaviors and PTSD Symptoms, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
91 participants
Enrollment target
3
Study locations

Study Summary

The overall goal of this work is to adapt, refine, and conduct an open trial of a parent-training intervention for Veterans with posttraumatic stress disorder (PTSD) symptoms using feedback from Veterans, VA clinicians, and expert consultants as key stakeholders. PTSD symptoms are associated with parent-child functioning difficulties, which are also an important determinant of quality of life and functional recovery. This project will examine the feasibility and acceptability of an evidence-based group intervention to improve parenting behaviors, parenting satisfaction, and family functioning in Veteran parents with PTSD symptoms and who have children between the ages of 3 and 12. This intervention is derived from an existing evidence-based intervention to improve Veteran relationship functioning (Strength at Home; SAH), and it is informed by the Cognitive Behavioral Theory of Interpersonal Functioning and the Military Family Attachment frameworks for the association between PTSD and family functioning problems. The intervention also includes a pre-treatment Motivational Interviewing Assessment (MIA) to assist Veterans in strengthening and building motivation to change their parenting behaviors. The goals and change talk identified in the pre-treatment MIA are then referred to throughout the treatment. Groups are gender-specific, meaning that the investigators will pilot the treatment in separate groups of women and men Veterans.

Primary Outcome

The Client Satisfaction Questionnaire-8 (CSQ) assesses acceptability post-treatment. Eight items are scored on a 4-point scale inquiring about quality of services, treatment satisfaction, and willingness to recommend the treatment to others. Ratings are summed, with higher scores representing greater acceptability ratings (possible range 4-32). This measure is commonly used in both clinical trials and program evaluation, and has been shown to correlate with treatment attendance and outcomes. It

Interventions

  • BEHAVIORAL SAHP

Study Locations (3)

Texas

  • Austin Information Technology Center, Austin, TX - Austin
  • Central Texas Veterans Health Care System, Temple, TX - Temple
  • Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX - Waco

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2019-03-01
Est. Completion 2022-03-31
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT03403153 record still lists

NCT03403153 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 91 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 1 condition, with Parenting Behaviors and PTSD Symptoms appearing as the primary indexed condition, and to 1 intervention - of which SAHP is the first listed.

NCT03403153 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT03403153 about?

NCT03403153 is a clinical study titled "Parenting Strength At Home- Parents Pilot". The overall goal of this work is to adapt, refine, and conduct an open trial of a parent-training intervention for Veterans with posttraumatic stress disorder (PTSD) symptoms using feedback from Veterans, VA clinicians, and expert consultants as key stakeholders. PTSD symptoms are associated with pa...

What is the current status of trial NCT03403153?

This trial is currently completed. It is a NA study. The enrollment target is 91 participants. The study started on 2019-03-01. Estimated completion is 2022-03-31.

What conditions does trial NCT03403153 study?

This clinical trial studies the following conditions: Parenting Behaviors and PTSD Symptoms.

What interventions are being tested in trial NCT03403153?

The interventions under investigation include: SAHP (BEHAVIORAL).

Who is sponsoring clinical trial NCT03403153?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03403153 being conducted?

This trial has 3 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT03403153's enrollment target sits among peer trials

91 939th of 2000 higher than 1,060 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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

  • NCT02671448 · 91 participants · NA

    Pilot Trial of Homebound Stem Cell Transplantation

  • NCT04835857 · 91 participants

    Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices

  • NCT05184842 · 91 participants · Phase 2

    Metabolically Optimized, Non-cytotoxic Low Dose Weekly Decitabine/Venetoclax in MDS and AML

  • NCT05685173 · 91 participants · Phase 1

    A Trial to Study if REGN5837 in Combination With Odronextamab is Safe for Adult Participants With Aggressive B-cell Non-Hodgkin Lymphomas

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

Source: ClinicalTrials.gov NCT03403153, the US trial registry maintained by the National Library of Medicine. NCT03403153 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.