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

NCT01817712 · ClinicalTrials.gov registry record · NA

Veterans Individual Placement and Support Towards Advancing Recovery

A NA study, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
541
Enrollment target

NCT01817712: Completed NA study, sponsored by VA Office of Research and Development.

NCT01817712 is a NA study that has completed, run by VA Office of Research and Development. The registered enrollment target is 541 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01817712, a NA study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
541 participants
Enrollment target

Study Summary

The primary objective of CSP#589 VIP-STAR is to evaluate the effectiveness of Individual Placement \& Support (IPS) in unemployed Veterans with PTSD. The primary hypothesis is that, compared to those treated with transitional work program (TWP), unemployed Veterans with PTSD treated with IPS will be significantly more likely to become a steady worker. A steady worker is defined as holding a competitive job for greater than or equal to 50% of the 18-month study follow-up period (i.e., greater than or equal to 39 of the 78 weeks). All participants will be followed for 18 months post-randomization. 12/14/12: Analytic plan augmented to allow for a sensitivity analysis of the primary outcome that would exclude the first 12 weeks post-randomization, and evaluate between group proportion of steady worker status, as defined by working in a competitive job for greater than or equal to 50% of the weeks during week 13-78. 7/1/13: Analysis plan has been augmented to include a logistic regression analysis of the primary outcome, adjusted for participating medical center. 10/4/13: Addition of the IPS-25 Fidelity Scale. The addition of the IPS-25 scale should increase the validity of study results. 1/15/15: Addition of an Interactive Voice Recognition/Web-based (IVR/Web) System; as an option for weekly data capture of the primary outcome data (employment history). 8/17/15: Approval of Supplemental Data Collection at Participant Study Exit; use of the data collected will supplement the study analysis plan and, provide further insight into the impact of vocational rehab. A Participant Satisfaction Survey will allow study participants to indicate their level of satisfaction with the study, vocational rehabilitation intervention and, suggestions for future research.

Primary Outcome

The primary outcome will be achievement of a "steady worker" status, defined as obtaining and maintaining competitive employment for at least 50% of the active follow-up period (i.e., greater than or equal to 39 weeks).

Interventions

  • BEHAVIORAL Individual Placement & Support
  • BEHAVIORAL VA Transitional Work Program

Trial Details

FieldValue
Enrollment Target 541 participants
Start Date 2013-12-31
Est. Completion 2017-02-03
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT01817712 record still lists

NCT01817712 is an interventional study that assigns participants to a tested intervention. The registered 541 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 2 interventions - of which Individual Placement & Support is the first listed.

NCT01817712 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01817712 about?

NCT01817712 is a clinical study titled "Veterans Individual Placement and Support Towards Advancing Recovery". The primary objective of CSP#589 VIP-STAR is to evaluate the effectiveness of Individual Placement \& Support (IPS) in unemployed Veterans with PTSD. The primary hypothesis is that, compared to those treated with transitional work program (TWP), unemployed Veterans with PTSD treated with IPS will be...

What is the current status of trial NCT01817712?

This trial is currently completed. It is a NA study. The enrollment target is 541 participants. The study started on 2013-12-31. Estimated completion is 2017-02-03.

What interventions are being tested in trial NCT01817712?

The interventions under investigation include: Individual Placement & Support (BEHAVIORAL), VA Transitional Work Program (BEHAVIORAL).

Who is sponsoring clinical trial NCT01817712?

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

How this trial's enrollment target compares

Where NCT01817712's enrollment target sits among peer trials

541 187th of 2000 higher than 1,814 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

  • NCT04929223 · 542 participants · Phase 1

    A Study Evaluating the Safety and Efficacy of Targeted Therapies in Subpopulations of Patients With Metastatic Colorectal Cancer (INTRINSIC)

  • NCT05584670 · 542 participants · Phase 1

    A First-in-human, Dose Escalation and Dose Expansion Study of SAR445877 in Adult Participants With Advanced Solid Tumors

  • NCT04557462 · 540 participants · Phase 3

    A Rollover Extension Program (REP) to Evaluate the Long-term Safety and Tolerability of Open Label Iptacopan/LNP023 in Participants With Primary IgA Nephropathy

  • NCT04956640 · 540 participants · Phase 1

    Study of LY3537982 in Cancer Patients With a Specific Genetic Mutation (KRAS G12C)

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 NCT01817712, the US trial registry maintained by the National Library of Medicine. NCT01817712 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.