Options for Pain Management Using Nonpharmacological Strategies

Study acronym: OPTIONS
StatusRecruiting
PhaseNot applicable
Started

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Trial flagged as At Risk
Primary completion moved at least 7 months later across 2 updates Jun 30, 2026 → Jan 31, 2027
See other at-risk trials from VA Office of Research and Development

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Primary completion pushed from Sep 30, 2026 to Jan 31, 2027
    • Study completion pushed from Oct 31, 2026 to Sep 30, 2027
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 3 of 7 entries
  2. Minor Primary completion pushed from Jun 30, 2026 to Sep 30, 2026
    • Eligibility criteria revised
    v10
  3. Minor Primary completion pushed from Mar 31, 2026 to Jun 30, 2026
    • Site contact updated
    v9
  4. Minor Primary completion date: Dec 31, 2025 to Mar 31, 2026
    • Site contact updated
    v8
  5. Minor Site contact updatedv7
Show 5 earlier versionsHide 5 earlier versions
  1. Minor Site contact updatedv6
  2. Minor Secondary endpoints: 6 to 7v5
  3. Minor Study title revisedv4
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v3
  5. Minor Study sites: 0 to 1
    • Study description expanded, about 2 words
    v2
  1. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to help Veterans learn about different ways they can manage chronic pain that do not involve medications. Veterans will work with a coach to explore the Veterans' values and goals and how different non-medication approaches may fit into these values and goals.
Trial Details
NCT Number NCT05563792
Lead Sponsor VA Office of Research and Development
Conditions
(from sponsor)
Pain
Related terms Agnosia, Chronic Pain, Pain
Enrollment 296 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov