Chronic Pain, Musculoskeletal Pain
Conditions
Keywords
Exercise Therapy, Multimodal exercise
Brief summary
Analyze the effectiveness of a multimodal circuit exercise program on chronic musculoskeletal pain and disability in older adults.
Detailed description
This is a randomized parallel study (two arms) with blinded outcome assessments. The participants' recruitment will be done by a non-probabilistic sampling resulting from invitations to Basic Health Units. The sample size estimation indicated 164 participants. Participants will be allocated, by means of a randomization process, to one of two groups (82 for each group): Experimental Group (multimodal circuit exercise) or Control Group (cycle of multidisciplinary lectures on pain ). The primary outcomes are global chronic pain intensity and global functional disability scores. The secondary outcomes are functional mobility and cardiorespiratory capacity. All analyses will be processed using the RStudio software. The differences will be considered statistically significant when a 2-tailed p-value is less than 5% (p \< 0.05). The statistical analysis will follow the intention to treat. Discussion: This study will discuss the effects of multimodal circuit exercise on global chronic pain intensity and global body functional disability scores. The hypothesize is that multimodal exercises will reduce musculoskeletal chronic pain and disability in older adults to the same extent as traditional supervised and structured exercises.
Interventions
OTHERMultimodal circuit exercise
A structured and supervised multimodal exercise circuit twice a week, under 12 weeks program. The circuit workout program consists of 8 exercises, divided into motor coordination, balance, strength, and aerobic exercises. The exercises will be employed in a reserved room inside of the Basic Health Units. The sessions of exercises will last approximately 50 minutes,
OTHERMultidisciplinary lectures
Multidisciplinary lectures on pain and usual care provided by the Basic Health Units. A cycle of multidisciplinary lectures on pain will be offered by professionals in physical education, nursing, physiotherapy, medicine, psychology and social work that will take place in the Basic Health Units every 15 days.
Sponsors
Federal University of Minas Gerais
Federal University of Tocantins
Universidade Federal de Goias
University of Brasilia
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
Another researcher collaborator (blinded) will be carried out the outcomes investigated.
Intervention model description
This is a randomized parallel study (two arms) with blinded outcome assessments.
Eligibility
Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Subjects from both sexes; * Aged 60 or higher; * Had a history of chronic pain in at least one synovial joint for more than three months.
Exclusion criteria
* Participants with some types of co-morbidities that may interfere with the research parameters, such as a history of stroke, stenosis of the spinal canal, severe heart disease, fibromyalgia, rheumatoid arthritis; * Participants who presented a level of pain between 7 and 10 points on the Numeric Rate Scale (NRS) in any body location; * Participants being under psychiatric treatment with sensory deficits (visual, auditory and intellectual) * Participants performing any supervised and structured exercise at the moment of study enrollment or six months before.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change on pain intensity. | Change from Baseline at immediately post-intervention | Will be used the Brief Pain Inventory (BPI). The Brief Pain Inventory (BPI) \[32, 33\]- a multidimensional, easily used questionnaire, aiming to diagnose a patient's chronic pain during the last 24 hours, categorized into 11 questions, scaled from 0 to 10, in which 10 indicates worst pain imaginable. |
| Change on disability. | Change from Baseline at immediately post-intervention | Will be used the Independence Index in Activities of Daily Living (Katz Index - KI). The total KI score is in the range 0 to 6, whose score 6 represents an independent patient and 0 indicates a highly dependent patient. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change on cardiorespiratory capacity. | Change from Baseline at immediately post-intervention | Will be used the 6-minute walk test. |
| Change on functional mobility | Change from Baseline at immediately post-intervention | Will be used the Time up and go test. |
Countries
Brazil
Outcome results
None listed