# FamilyLive Feasibility and Effectiveness Study

> **NCT01524185** · EARLY_PHASE1 · WITHDRAWN · sponsor: **Hugo W. Moser Research Institute at Kennedy Krieger, Inc.**

## Conditions studied

- Mood Lability
- PTSD
- Anxiety

## Interventions

- **BEHAVIORAL:** FamilyLive
- **BEHAVIORAL:** Standard Mental Health Treatment

## Key facts

- **NCT ID:** NCT01524185
- **Lead sponsor:** Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
- **Sponsor class:** OTHER
- **Phase:** EARLY_PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** 2009-02
- **Primary completion:** 2016-01-08
- **Final completion:** 2016-01-08
- **Target enrollment:** 0 (ACTUAL)
- **Why stopped:** There were not enough eligible families and trained clinicians to conduct RCT.
- **Last updated:** 2018-04-09

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01524185

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01524185, "FamilyLive Feasibility and Effectiveness Study". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT01524185. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
