Loading
PTSD / Parenting-STAIR Modular (PSTAIR-M) / Treatment as Usual (TAU) · Interventional Study
ClinicalTrials.gov · August 7, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a prospective, interventional registry record for an ongoing trial comparing a modular trauma-focused parenting intervention (PSTAIR-M) to treatment as usual in military-connected mothers with PTSD and depression. No efficacy data are reported in this registry entry; the study is in active recruitment and will measure PTSD (PCL-5), depression (PHQ-9), and parenting competence (PSOC) at baseline, mid-treatment (11 weeks), and post-treatment (17 weeks).
Interventional, Randomized, Parallel, Single masking, Treatment purpose. PTSD, Depression, Parent-Child Relations; Female; age from 18 Years. Intervention: Parenting STAIR Modular (PSTAIR-M). Compared with: Treatment as Usual (TAU) — Active Comparator. n = 120. 3 sites: United States.
This is a prospective, interventional registry record for an ongoing trial comparing a modular trauma-focused parenting intervention (PSTAIR-M) to treatment as usual in military-connected mothers with PTSD and depression. No efficacy data are reported in this registry entry; the study is in active recruitment and will measure PTSD (PCL-5), depression (PHQ-9), and parenting competence (PSOC) at baseline, mid-treatment (11 weeks), and post-treatment (17 weeks).
This is a registry record only; no efficacy or safety results are reported.
Once results become available, this study may help clinicians determine whether a modular, trauma-informed parenting intervention improves maternal mental health and parenting capacity in military families. Until outcomes are reported, no clinical recommendation can be made.
This is a registry record for an ongoing recruitment-phase trial of an adapted trauma-focused parenting intervention; no results are reported, making it an early-stage feasibility and efficacy study.
As stated by the source record.
Quoted from the source exactly as published.
Once results become available, this study may help clinicians determine whether a modular, trauma-informed parenting intervention improves maternal mental health and parenting capacity in military families. Until outcomes are reported, no clinical recommendation can be made.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06262178). This is a study registration, not published results. Lead sponsor: New York University. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 120 participants (ESTIMATED). Conditions: PTSD, Depression, Parent-Child Relations. Interventions: BEHAVIORAL: Parenting-STAIR Modular (PSTAIR-M); BEHAVIORAL: Treatment as Usual (TAU). Primary outcome measures: Post-traumatic stress disorder (PTSD) Checklist 5 , PCL-5 will be administered at three assessment timepoints: pre-treatment (baseline), mid-treatment (after session 11, approximately 11 weeks after baseline), and post-treatment (approximately 17 weeks after baseline).; Patient Health Questionnaire-9 (PHQ-9) , PHQ-9 will be administered at three assessment timepoints: pre-treatment (baseline), mid-treatment (after session 11, approximately 11 weeks after baseline), and post-treatment (approximately 17 weeks after baseline).; Parenting Sense of Competence Scale (PSOC) , PSOC will be administered at three assessment timepoints: pre-treatment (baseline), mid-treatment (after session 11, approximately 11 weeks after baseline), and post-treatment (approximately 17 weeks after baseline).. Brief summary: The goal of this study is to assess Parenting STAIR Modular (PSTAIR-M), a promising and innovative intervention for military-connected mothers (MCM) who have experienced trauma and their young children (ages 2-10). PSTAIR-M aims to help mothers manage the strong feelings that sometimes happen after experiencing something scary or stressful, as well as to better connect with their children and manage their behavior effectively. The main questions the study aims to answer are: 1) Does PSTAIR-M reduce maternal PTSD and/or depression symptoms?, and 2) Does PSTAIR-M improve parental functioning? Researchers will compare PSTAIR-M to treatment as usual (TAU) - other EBTs offered at participating study sites - to determine if PSTAIR-M is more effective in improving mental health and parenting. Participants will: 1) attend 12-16 weekly, 1-hour online treatment sessions with their assigned clinicians, 2) complete three 1-hour online assessments administered by research staff, 3) engage with their child in three 15-30-minute online, observed play sessions, 4) have assessments and observed play sessions audio and video recorded. Participants may also be invited to participate in an optional, 30-minute online one-on-one qualitative interview, which would be audio and video recorded and would cover participants' experiences with the intervention, the clinic sites, and their providers.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.