Community-Engaged Options to Facilitate Opioid Reduction

NCT ID: NCT05098158

Last Updated: 2025-10-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 21 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-10
• Study Completion Date: 2022-01-03

Brief Summary

This study investigates how adults prescribed opioids for chronic noncancer pain respond to invitations to try non-opioid options of massage therapy, yoga therapy, chiropractic and physical therapies. Options will be available via telehealth consultation visits using a computer or smartphone with internet connection. The investigators will measure effects on pain, pain-related symptoms, and opioid use over time using a single-group design.

Detailed Description

Participants will be recruited from local primary care practices and asked to complete a baseline survey. They will then meet with a registered nurse via teleconference for a complete pain assessment. At the end of the session, participants will be asked to choose two of four available modalities for telehealth consultation. Participants will be scheduled for six telehealth sessions, once per week x six weeks with three consultations per each chosen therapy. Measurements of pain, mood, sleep, medicine use will be captured at baseline, three weeks and six weeks and examined for changes over time.

Conditions

Chronic Pain

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Single arm pain treatment

Arm includes usual pain care plus the chosen two telehealth interventions x 6 weeks

Group Type: EXPERIMENTAL

Non-pharmacological pain treatment

Intervention Type: OTHER

Participant selects from telehealth consultation on massage therapy, yoga therapy, chiropractic and physical therapies.

Interventions

Non-pharmacological pain treatment

Participant selects from telehealth consultation on massage therapy, yoga therapy, chiropractic and physical therapies.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• enrollment in treatment at the CHAS Perry St or partnering clinic;
• age greater than 18 years;
• ability to read, speak, and write English;
• diagnosed with a chronic, non-cancer-based painful medical condition;
• ability to provide informed consent.

Exclusion Criteria

• pregnancy;
• diagnosis of a cancer-based painful medical condition;
• any other medical or psychiatric condition that the PI or Co-PI physician of record determine might compromise safe study participation (including but not limited to active psychosis, history of frequent psychiatric hospitalizations, severe anxiety with claustrophobia, aggression)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Spokane Regional Health District

UNKNOWN

Sponsor Role: collaborator

University of Washington Institute for Translational Health Science (KL2)

OTHER

Sponsor Role: collaborator

Rayce Rudeen Foundation

UNKNOWN

Sponsor Role: collaborator

Washington State University

OTHER

Sponsor Role: lead

Responsible Party

Marian Wilson

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Community Health Association of Spokane

Spokane, Washington, United States

Washington State University College of Nursing

Spokane, Washington, United States

Countries

United States

Provided Documents

Document Type: Study Protocol, Statistical Analysis Plan, and Informed Consent Form

View Document

Other Identifiers

18111

Identifier Type: -

Identifier Source: org_study_id