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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06077526
Other study ID # 23-010
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 13, 2026
Est. completion date May 15, 2027

Study information

Verified date February 2024
Source Bridgewater College
Contact Michael Ray, DC, MSc
Phone 540-828-5416
Email bray@bridgewater.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic musculoskeletal pain (CMP) and lack of physical activity often co-exist, contributing to increased disability, non-communicable diseases (e.g., obesity, diabetes, hypertension), psychological comorbidity (e.g., anxiety and depression), and healthcare utilization and costs [1-6]. Many individuals with CMP seek assistance at emergency departments (ED). ED overuse has been an ongoing concern, with 1-in-5 Americans presenting to the ED at least once each year [7]. Of these visits, 24 million are for adults seeking help for chronic pain, with an additional 12 million due to exacerbations of an existing chronic pain condition [8]. In 2021, the fourth most common reason for seeking care in the ED related to a primary diagnosis involving the musculoskeletal system, with an estimated 9.5 million visits [9]. Most ED visits result in a 'treat and release' approach, potentially disrupting continuity of care and resulting in follow-up ED visits [10]. These ED visits for chronic pain are indicative of accessibility problems to community-based primary and preventative care, compounded by limited or no health insurance coverage [10]. Based on the Emergency Medical Treatment and Labor Act, EDs are required to stabilize all patients regardless of ability to pay [10]. To alleviate the burden of CMP on patients and EDs, improve access to quality healthcare, and mitigate initial and repeat ED visits, alternative options are required. Here we propose a novel group-based intervention involving pain education (PE) and physical activity (PA) implemented in CMP patients presenting to the ED of a community level hospital. The investigators will recruit 60 adults from a community hospital located in the Shenandoah Valley region of Virginia; participants will be randomized to either Pain Education and Active Knowledge (P.E.A.K.) Rx (24 sessions of group PE+ + PA) or usual care. Research assessments are conducted with both groups at study entry (baseline), 8-weeks, 3-months, and 6-months.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date May 15, 2027
Est. primary completion date May 15, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years of age or older - Sedentary (e.g., not meeting PA guidelines, assessed by ACSM PA vitals) - English speaking and reading comprehension - Not currently pregnant - Diagnosed with CMP based on electronic health record: - Non-red flag presentation (e.g., red flags: current fracture, malignancy, infection, vascular issues, or in need of surgical intervention). - Persistent or recurrent pain for 3+ months, with at least moderate pain intensity level (Visual Analog Scale of 40/100)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
P.E.A.K. Rx
Pain Education + Physical Activity Group Based Intervention
Other:
Usual Care
Participants will receive the community hospital's usual care.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bridgewater College

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scale Quantitative metric of an individual's pain on a numerical scale. Scores range from 0 - 100, where 0 means no pain and 100 means maximum pain.
1-30 = mild 31-69 = moderate 70-100 = severe MCID of 12 point change [60].
Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary Tampa Scale of Kinesiophobia Quantitative metric asking 17 questions using a 4-point Likert scale regarding a participant's fear and avoidance of movement. Scores range from 17 to 68, where 17 means no kinesiophobia and higher scores indicate increasing severity of kinesiophobia. Scores = 37 indicate kinesiophobia. MCID of 7.5-9 points [61]. Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary Pain Catastrophizing Scale 13-item quantitative metric assessing participant's catastrophic thinking about their pain experience, contributing to rumination, magnification, and learned helplessness. Utilizes 4-item scale to assess frequency of particular thoughts, 0 = not at all to 4 = all the time. Total score ranges from 0 - 52. Score = 30 indicates catastrophizing.
MCID of 11 points for those considered to be engaging in catastrophic thinking (baseline score >30 points) [62].
Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary Patient Specific Functional Scale (PSFS) Assesses impact of pain on participant's function by identification of difficult or unable to perform activities. 11-point Likert scale ranks participant's current level of difficulty for each activity (0 = unable to perform, 10 = able to perform activity at same level before injury or problem).
Assess improvement in function of valued activities post intervention. MCID is categorized:
Small change = 1.3 Medium change = 2.3 Large change = 2.7 [63].
Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary Saltin-Grimby physical activity scale for leisure time physical activity Assesses participants perception of their leisure time activities. Describe your exercise and physical exertion in leisure time. If your activity varies much, for example between summer and winter, then give an average. The question refers only to the last year.
Four different levels:
"Reading, watching TV, or other sedentary activity," "Walking, cycling, or other forms of exercise at least 4 hours a week (here including walking or cycling to place of work, Sunday walking, etc.)," "Participation in recreational sports, heavy gardening, etc. (note: duration of activity at least 4 hours a week)" and "Participation in hard training or sports competitions, regularly several times a week." 4 levels renamed: "inactive," "low," "moderate," and "vigorous," respectively [65]
Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary 36-Item Short Form Health Survey (SF-36) A health-related quality of life survey assessing eight dimensions: physical function, role limitations due to physical health problems, bodily pain, general health, vitality, social functioning, role limitation due to emotional problems, and mental health. Scores for each dimension range from 0 (worst level of functioning) to 100 (best level of functioning). Total sore MCID of 4.6 points [64]. Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary Self-report physical exercise Exercise assessment through 3 questions on frequency, duration, and intensity, where the respondents will be asked to estimate their weekly average. Frequency question: "How often do you exercise (i.e., walking, skiing, swimming or training/sports)?" Duration question: "For how long (time) do you exercise?" Intensity question "If you exercise-how hard do you exercise?"
Frequency categories:
"never", "less than once a week", "once a week", "2 to 3 times a week", or "approximately every day".
Duration categories:
"less than 15 minutes", "15 to 29 minutes", "30 to 60 minutes", or "more than 1 hour."
Intensity categories:
"Easy-you do not become short-winded or sweaty", "You become short-winded and sweaty", and "Hard-you become exhausted". Categorized as "low", "moderate", and "hard" respectively [65].
Baseline, post-intervention 8-weeks, 3-months, and 6-months
Secondary Self-report occupational activity Assess occupational physical activity.
Question: "If you have paid or unpaid work, which statement describes your work best? Response categories:
"mostly sedentary work (e.g., office work)", "work that requires a lot of walking (e.g., shop assistant, light industrial work)", and "work that requires a lot of walking and lifting (e.g., nursing, construction, or heavy manual labor)".
Baseline, post-intervention 8-weeks, 3-months, and 6-months
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