Chronic Musculoskeletal Pain Clinical Trial
Official title:
Efficacy of the Transition of the Foot Strike Pattern From Rearfoot to Midfoot or Forefoot During Running on Pain and Disability in Cadets With Chronic Musculoskeletal Pain
NCT number | NCT04166136 |
Other study ID # | TFSP |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | June 15, 2019 |
Est. completion date | August 30, 2020 |
Verified date | October 2022 |
Source | Centro Universitário Augusto Motta |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To investigate the efficacy of the footstrike pattern transition from rearfoot to midfoot / forefoot pattern compared to lower limb muscle strengthening exercises and lumbar spine region on decreasing the intensity of chronic musculoskeletal pain in cadets from Naval School. Methods: A randomized controlled trial with blind evaluator and allocation of participants in three parallel groups will be performed. Participating in the study, 81 cadets of the Naval Academy of Rio de Janeiro, between 18 and 24 years of age with chronic musculoskeletal pain in the lower limbs or in the lumbar region and who have the rearfoot as footstrike pattern. Participants will be randomly assigned into the following groups: (1) footstrike pattern transition from rearfoot to midfoot / forefoot; (2) muscle strengthening of the lower limbs and lower back; and (3) usual treatment group. Primary treatment outcomes will be pain and specific disability measured twelve weeks after randomization. Secondary treatment outcomes will be pain and specific disability measured six and nine months after randomization. An intention-to-treat analysis will be performed using mixed linear models to compare outcomes between groups.
Status | Terminated |
Enrollment | 25 |
Est. completion date | August 30, 2020 |
Est. primary completion date | August 30, 2020 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years to 25 Years |
Eligibility | Inclusion Criteria: 1. chronic musculoskeletal pain in the lower limbs and / or non-specific chronic low back pain that is related to running ("persistent pain" will be considered "chronic" for more than three months). Information on pain will be based on a self-completion questionnaire; 2. rearfoot as a foot strike pattern; 3. present at least one run-related limitation on the Specific Functional Scale of the Patient (EFEP); 4. practice running 2 to 5 times a week. Exclusion Criteria: 1. have undergone a surgical procedure in the lower limbs and / or the lower back in the last six months; 2. have performed invasive procedures for pain relief in the last three months; do not present a history of acute trauma such as fractures in the last six months, infection, signs of radiculopathy, compression of the marrow or equine tail. |
Country | Name | City | State |
---|---|---|---|
Brazil | Centro Universitário Augusto Motta | Rio de Janeiro | |
Brazil | UNISUAM | Rio de Janeiro | RJ |
Lead Sponsor | Collaborator |
---|---|
Centro Universitário Augusto Motta | Naval School |
Brazil,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain intensity: Brazilian version of the Numerical Pain Scale | Pain intensity will be measured using the Brazilian version of the Numerical Pain Scale,whose ranges from 0 to 10, where 0 represents "no pain" and 10 represents "the worst possible pain" based on the last seven days. | Three months after randomization | |
Primary | Specific disability | Specific disability through the Patient Specific Functional Scale. At this scale, the participant should report three activities whose achievements are being hampered by pain. Participant should note the difficulty on a scale of 0 to 10, where 0 means "unable to perform activity" and 10 means "able to perform the activity as you did before the injury." | Three months after randomization | |
Secondary | Weekly running mileage | Weekly running mileage will be obtained through a self-completion questionnaire in which participants will answer the following question: "How many kilometers do you run per week?". | Three months after randomization | |
Secondary | Weekly running mileage | Weekly running mileage will be obtained through a self-completion questionnaire in which participants will answer the following question: "How many kilometers do you run per week?". | Six months after randomization | |
Secondary | Pain intensity: Brazilian version of the Numerical Pain Scale | Pain intensity will be measured using the Brazilian version of the Numerical Pain Scale,whose ranges from 0 to 10, where 0 represents "no pain" and 10 represents "the worst possible pain" based on the last seven days. | Six months after randomisation | |
Secondary | Specific disability | Specific disability through the Patient Specific Functional Scale. At this scale, the participant should report three activities whose achievements are being hampered by pain. Participant should note the difficulty on a scale of 0 to 10, where 0 means "unable to perform activity" and 10 means "able to perform the activity as you did before the injury." | Six months after randomisation |
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