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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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11 April 2016 |
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Main ID: |
NCT02235207 |
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Date of registration:
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05/09/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Effectiveness of Fustra—Exercise Program in Neck and Low Back Pain
FUSTRA |
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Scientific title:
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Effectiveness of Fustra—Exercise Program on Pain, Physical Fitness and Quality of Life in Female and Male Office Workers Suffering From Recurrent Neck and Low Back Pain — a Randomized Controlled Trial |
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Date of first enrolment:
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September 2014 |
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Target sample size:
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175 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02235207 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Finland
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Contacts
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Name:
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Jaana H Suni, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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UKK Institute |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- age 30-50 years
- sedentary "office" worker sitting at least 6 hours per day
- rating of neck pain or low back pain in the past four weeks is at least 3 in 10 point
scale (1-10)
- number of pain episodes (neck/back) in the past year is at least 2
Exclusion Criteria:
- chronic pain (neck/back) defined as continuous pain over 1 year
- serious former neck injury (fracture, surgery, whiplash, protruded disc)
- serious former back injury (fracture, surgery, protruded disc)
- engaged in neuromuscular exercise 3 times a week or more
- engaged in competitive sports
- pregnant
Age minimum:
30 Years
Age maximum:
50 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Low Back Pain, Recurrent
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Neck Pain
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Intervention(s)
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Behavioral: Neuromuscular exercise
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Primary Outcome(s)
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Change in the intensity of pain in the neck or/and low back
[Time Frame: Baseline, 12 months]
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Secondary Outcome(s)
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Change in the intensity of pain in the neck or/and low back
[Time Frame: Baselilne, 3 months]
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Change in musculoskeletal fitness index
[Time Frame: Baselilne, 3 months]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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