PREDICT-DOLOR VE: Validation of a Structured Triage Protocol for Chronic Pain
- Sponsor
- Universidad Central de Venezuela
- Study ID
- NCT07696676
- Status
- Not Yet Recruiting
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Conditions
- Chronic Pain
- Neuropathic Pain
- Pain Management
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 100 Years
- Healthy Volunteers
- Not accepted
Interventions
- PREDICT-DOLOR VE — OTHERA structured, rule-based clinical decision support tool integrating five validated pain assessment instruments (Numeric Rating Scale, Douleur Neuropathique 4, Brief Pain Inventory, Pain Catastrophizing Scale, and Patient Health Questionnaire-9) to generate a four-level triage recommendation for chronic pain management, operating on a free digital platform with no implementation cost.
Study Details
PREDICT-DOLOR VE is a structured clinical triage protocol for chronic pain that uses five internationally validated pain assessment instruments to help healthcare providers determine the appropriate level of care for patients with chronic pain. The tool operates on a free mobile-friendly platform and generates a four-level recommendation: primary care management, referral to physiatry or neurology, priority specialist evaluation, or evaluation for neurosurgical intervention. This study will validate the diagnostic accuracy of the PREDICT-DOLOR VE algorithm by comparing its recommendations with the independent assessment of a panel of three specialists in adult patients with chronic pain (lasting 3 months or longer) across three referral centers in Venezuela. The study aims to determine whether this structured, low-cost approach can help connect patients with the right type of care more quickly and consistently.
Key Dates
- First listed
- Jul 10, 2026
- Start date
- Aug 1, 2026
- Status verified
- Jul 2026
- Primary completion
- Dec 2, 2026
- Completion
- Feb 2, 2027
Study Design
- Enrollment
- 120 participants (estimated)
Arms
- Arm: Chronic pain patientsConsecutive adult patients (18 years and older) with chronic pain of any etiology lasting 3 months or longer, evaluated at three referral centers in Venezuela. All patients complete the PREDICT-DOLOR VE digital assessment battery (NRS, DN4, BPI, PCS, PHQ-9) and receive an independent consensus evaluation from a panel of three specialists blinded to the algorithm's recommendation.
Primary Outcome Measure
At completion of each patient's assessment (single visit, approximately 15-20 minutes) [ Time Frame: At completion of each patient's assessment (single visit, approximately 15-20 minutes) ]
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