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Impact of Home Exercise Delivery on Compliance & Outcomes for Musculoskeletal Pain

The Impact of Home Exercise Program Delivery Type on Exercise Compliance and Clinical Outcomes for Musculoskeletal Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03470753
Enrollment
116
Registered
2018-03-20
Start date
2018-01-12
Completion date
2019-11-30
Last updated
2020-01-18

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

Conditions

Chronic Low Back Pain, Chronic Pain, Compliance, Patient, Knee Pain Chronic

Brief summary

Patients seeking care for chronic low back or knee pain will be recruited for enrollment, and randomized within two phases (retention and compliance). Patients will consent to a 2-step study design, with independent randomization for each. The initial step will assess retention based on 4 different exercise prescription strategies. This will be assessed short-term, and then the 2nd step will consist of a second independent randomization to receive different reminder strategies to determine their influence on exercise compliance at home.

Detailed description

Patients seeking care for their chronic low back or knee pain will be recruited to participate in a trial investigating the value of different exercise and education prescription strategies as well as strategies to determine the influence of various exercise reminder strategies. On day 1 of enrollment, patients will be randomized and instructed in two different types and amounts of exercises, as well as two types of delivery strategies. The ability to recall and perform these exercises will be assessed 20 minutes after completion of the instructional period (retention). In phase 2, patients will be randomized to receive different reminder strategies (none, email, text, and/or video) and their compliance assessed over a 1 month period (compliance). Self-reported compliance over the first month, and health care utilization outcomes will be analyzed for the 1 year following completion of the 1 month period, in all groups.

Interventions

OTHERNumber of Exercises

Subjects will receive either 2 or 4 exercises to evaluate the short-term recall and performance.

OTHERType of Instruction

The type of instruction in phase 1 will be compared: Instruction by providing a handout only vs being instructed by a provider and practiced by the patient with provider feedback.

OTHERDelivery Type

In phase 2 subjects will be provided 4 exercises using only a handout vs delivered to them electronically with the addition of a video.

OTHERMobile Reminder

A text-message based mobile reminder tool will be utilized to engage with subjects via texting on a daily basis to provide reminders and encouragement to perform their home exercises.

Sponsors

Dan Rhon
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. The primary complaint of low back pain or knee pain and is not actively seeking care for their contralateral knee. 2. The current episode for the injury is 6 weeks or greater 3. A home exercise program is appropriate as part of the management plan for their injury on the first day 4. Between the age of 18 and 65 years. 5. Own and utilize a smart phone 6. Read and speak English well enough to interact with the smart phone-based tool. 7. Able and willing to come in for follow-up at 1-month.

Exclusion criteria

1. History of prior surgery to the lower extremities or spine 2. Already receiving or have received treatment for this episode of pain within the past 6 months. 3. Medical red flags of a potentially serious condition including cauda equina syndrome, major or rapidly progressing neurological deficit, fracture, malignancy, joint infection, or systemic disease 4. If participating with low back pain, known current pregnancy or history of pregnancy in the last 6 months 5. Exiting military health system in the next 2 months, pending litigation, or pending a medical separation board.

Design outcomes

Primary

MeasureTime frameDescription
Performance Assessment Tool1-monthA locally developed tool designed to meet the needs of assessing both exercise retention and compliance. It will capture the subject's ability to recall the name of an exercise, the prescribed sets and repetitions, and the ability to perform an exercise using a 4-point ordinal scale
Compliance1-monthSubjects will be asked to submit self-reported daily compliance logs.

Secondary

MeasureTime frameDescription
Patient Reported Outcomes Measurement Information Systems (PROMIS) 57 (v2.0)1-monthThe PROMIS 57-item short form efficiently assesses several outcomes important to patients with chronic low back and knee pain including pain intensity and interference, sleep disturbance, anxiety, depression, fatigue, and social role participation using items developed with rigorous methodology and patient input.
Patient Acceptable Symptom State (PASS)1-monththe PASS as a global, dichotomized single-item score indicating if patients are satisfied with the current state of their symptoms.
Self-perception on Physical Health and Ability to Return to Work or Full Duty1-monthThis survey consists of a total of 9 questions, 5 of them modified from the Short Form-36. It asks questions related to the subject's perception of their physical health. The first 5 questions are related to the subject's perception of ability to return to work or full duty, the need for additional healthcare for their current condition, and function at the level that they feel is expected of them. The final 4 questions ask about their perception of general physical health.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026