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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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16 December 2017 |
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Main ID: |
NCT03350867 |
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Date of registration:
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18/11/2017 |
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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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Effects of Using Customized Insoles With Anterior or Posterior Plantar Support in Cross-pelvis Syndrome and Perception of Body Alignment in Young Adults: a Randomized Clinical Trial
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Scientific title:
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Effects of Using Customized Insoles With Anterior or Posterior Plantar Support in Cross-pelvis Syndrome and Perception of Body Alignment in Young Adults: a Randomized Clinical Trial |
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Date of first enrolment:
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August 9, 2017 |
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Target sample size:
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15 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03350867 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Contacts
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Name:
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Eduardo Pimentel, Bachelor |
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Address:
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Telephone:
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+5581998040297 |
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Email:
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eduspimentel@hotmail.com |
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Affiliation:
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Name:
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Eduardo Pimentel, Bachelor |
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Address:
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Telephone:
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+5581998040297 |
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Email:
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eduspimentel@hotmail.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Crossed pelvis syndrome (anterior or posterior)
- Difference in length leg = 1cm
- Don't show: scoliotic or kyphotic deformity; chirurgie or fracture in spine in last 12
months; thoracic chirurgie; diabetic neuropathy; cesarean surgery; mixed crossed
pelvis syndrome
- Not participating in any physical activity or physiotherapy
Exclusion Criteria:
- Join in other physical activity during the study
- Refuse to wear the insoles
Age minimum:
18 Years
Age maximum:
25 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Crossed Pelvis Syndrome
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Intervention(s)
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Other: Personalized Insole Group
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Other: Placebo Group
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Primary Outcome(s)
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Posture
[Time Frame: 45 days]
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Secondary Outcome(s)
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Lombar colune mobility
[Time Frame: 45 days]
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Moviment amplitude (hip joint, knee)
[Time Frame: 45 days]
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Pain
[Time Frame: 45 days]
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Abdominal circunference
[Time Frame: 45 days]
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Sacroiliac mobility
[Time Frame: 45 days]
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Secondary ID(s)
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Insole and cross-pelvis synd.
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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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