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Self-Management of Chronic Low Back Pain: Targeting Patient Activation

Supporting Patient Activation for Self-Management of Chronic Low Back Pain With a Targeted Intervention Based on Key Influencing Characteristics

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06236529
Enrollment
34
Registered
2024-02-01
Start date
2022-07-16
Completion date
2023-04-11
Last updated
2024-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low-back Pain, Patient Activation

Keywords

Self-management, Nurse-led, Web-based

Brief summary

Patients with chronic low back (cLBP) pain report reduced physical function and ability to participate in social roles and are more likely to use opioid pain medications. While self-management interventions have been shown to support these patients, effectiveness has been limited due to poor patient engagement. Patient activation encompasses the skills, knowledge, and motivation that a person has to manage the person's health. Supporting patient activation may improve the effectiveness of self-management for cLBP. In this single-masked pilot study of adults with cLBP, patients were randomized to receive either no intervention (control) or 6 weekly sessions of an evidence-based web-based self-management program (SMP) with or without health behavior change counseling (HBCC) using motivational interviewing. Participants were assessed at baseline and at 12 and 26 weeks using the Patient Activation Measure, Oswestry Disability Index and Patient-Reported Outcomes Measurement Information System (PROMIS) physical function, social role participation, and pain interference. The investigators assessed acceptability and feasibility based on recruitment, session attendance, and follow-up.

Interventions

BEHAVIORALHealth Behavior Change Counseling

A telephone-based intervention employing principles and practices of motivational interviewing.

An evidence-based 6-week SMP led by a registered nurse. The SMP was based on the Arthritis Self-Management Program and the Chronic Disease Self-Management Program.

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The outcomes assessors were masked to treatment assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults (18+ years of age) * Seen in primary or specialty care practice for non-specific low back pain * Chronic low back pain per the NIH Task Force on Research Standards for cLBP * Worst back pain of at least 4/10 points * Oswestry disability index of at least 24% * English speaking

Exclusion criteria

* History of lumbar spine decompression/laminectomy or fusion surgery in the past 6 months * Possible non-musculoskeletal cause for LBP symptoms diagnosis at baseline * Red flag LBP diagnosis in the previous 6 months (e.g., cauda equina syndrome, osteomyelitis, or spinal neoplasm) * Neurological disorder resulting in moderate to severe movement dysfunction * Presence of any psychotic disorder

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of researchBaselineAcceptability - at least 50% of individuals approached agree to eligibility screening for the study, having at least 30% of those who were deemed eligible for the study agree to participate
Feasibility of studyBaselineFeasibility - (1) having at least 80% of enrolled participants attend at least 3 of the 6 scheduled self-management program sessions; and (2) having a loss to follow-up rate of \< 20% of enrolled participants over the 26-week study

Secondary

MeasureTime frameDescription
Patient Activation Measure (PAM) score12 weeksThe Patient Activation Measure (PAM) is a 13-item instrument where patients are provided 5 response options, ranging from strongly agree to strongly disagree. Based on their answers, patients were assigned a numerical score ranging from 0 (no activation) to 100 (highest activation), and the score was used to stratify patients into 1 of 4 stages of activation: stage 1 (believes taking an active role is important), stage 2 (has the confidence and knowledge to take action), stage 3 (takes action), and stage 4 (stays the course under stress)
Oswestry Disability Index (ODI) score12 weeksPain-related disability was assessed using the ODI, a 10-item measure of low back pain-related disability that evaluates the current effect of a patient's low back pain on various aspects of daily living. ODI scores range from 0 to 100, with higher scores indicating greater disability.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026