ACTRN12609000825257
Completed
未知
A randomised clinical trial on the effect of a comprehensive exercise program on average weekly pain intensity in chronic whiplash
The George Institute For International Health, The University of Sydney0 sites172 target enrollmentSeptember 22, 2009
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- The George Institute For International Health, The University of Sydney
- Enrollment
- 172
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Key inclusion criteria:
- •1\. Grade I or II whiplash of at least 3 months duration but less than 12 months duration.
- •2\. Currently experiencing at least moderate pain OR moderate activity limitation due to pain (modified items 7 \& 8 of SF36\).
- •3\. Not currently receiving care for whiplash.
- •4\. Aged between 18 years and 65 years old.
- •5\. Proficient in written and spoke English.
Exclusion Criteria
- •Key exclusion criteria:
- •1\. Known or suspected serious spinal pathology (e.g. metastatic disease of the spine).
- •2\. Confirmed fracture or dislocation at time of injury.
- •3\. Nerve root compromise.
- •4\. Spinal surgery in the past 12 months.
- •5\. Any coexisting medical condition which would severely restrict participation in the exercise program e.g. traumatic brain injury.
- •6\. Any of the contraindications to exercise listed in the American College of Sports Medicine (ACSM) guideline screened using the Physical Activity Readiness Questionnaire (PAR\-Q).
Outcomes
Primary Outcomes
Not specified
Similar Trials
Active, not recruiting
Not Applicable
Compare topical anesthetic patches, Rapydan versus EmlaVenipuncture, especially in children, is associated with pain and discomfort. For this reason, often use a local anesthetic.Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]EUCTR2011-000750-37-NLIsala Klinieken200
Completed
Phase 4
A randomised clinical trial on the effectiveness of Emla and Rapydan for prevention of vena punction-induced pain in children.PijnbelevingPain perception/ discomfortNL-OMON35993Isala Klinieken200
Active, not recruiting
Not Applicable
Efficacy of barrier cream with honey in the treatment of intertrigo.EUCTR2011-001469-42-NLDeventer Ziekenhuis60
Completed
Not Applicable
Clinical trial on the efficacy of an intervention package to improve adherence to treatment for systolic blood pressure (BP) reduction in primary care patients with poorly controlled or uncontrolled BPISRCTN21229328Health Service of the Balearic Islands (Servei de Salut de les Illes Balears [IB-salut]) (Spain)309
Completed
Not Applicable
A randomised clinical trial of the effectiveness of ventilation by Oxylator® EMX versus bag-valve device in pre-hospital emergency patientsMechanical ventilation needRespiratoryISRCTN20664878CPR Medical Devices Inc. (Canada)200