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One MORE for Chronic Pain in Latinos

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Enrolling

Conditions

Chronic Pain

Treatments

Behavioral: One MORE (Spanish Adaptation)

Study type

Interventional

Funder types

Other

Identifiers

NCT06316713
IRB_00166637

Details and patient eligibility

About

This study will be a single-site, two-arm randomized controlled trial conducted among Spanish-speaking chronic pain patients. Chronic pain patients will be randomized by a computer-generated randomization schedule with simple random allocation (1:1) to either One MORE or a wait-list control condition (WLC). One MORE will be delivered individually either in-person or via a HIPAA compliant virtual meeting platform.

Enrollment

34 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Spanish-speaking
  • Age 18+
  • Diagnosed with a chronic pain condition
  • Average pain in the previous week > or = 3
  • Willingness to participate in study interventions and assessments.

Exclusion criteria

  • Non Spanish-speaking
  • Score of 10 or greater ('high risk') on the suicidality subsection of the MINI
  • Psychotic episode within the last 12 months as deemed by the corresponding subsection of the MINI
  • Presence of clinically unstable illness judged to interfere with treatment or study procedures
  • Unable or unlikely to complete study procedures (e.g., planned major surgery, anticipated move, travel barrier)
  • Communication or cognitive impairment that limits participation in treatment or study procedures.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

34 participants in 2 patient groups

One MORE (Spanish Adaptation)
Experimental group
Treatment:
Behavioral: One MORE (Spanish Adaptation)
Waitlist Control
No Intervention group

Trial contacts and locations

1

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Central trial contact

Eric Garland, PhD; Carter Minnick, BA

Data sourced from clinicaltrials.gov

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