Effects of Two Techniques of Mobilization in the Dorsiflexion on Patients With Chronic Ankle Instability
This study has been completed.
Sponsor:
CEU San Pablo University
Information provided by (Responsible Party):
Angel Luis Rodriguez, CEU San Pablo University
ClinicalTrials.gov Identifier:
NCT01618032
First received: June 8, 2012
Last updated: November 30, 2012
Last verified: November 2012
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Purpose
Restrictions on ankle dorsiflexion are common in subjects with chronic ankle instability (CAI). In fact, this is one factor that can contribute to the recurrence of such injuries. Passive mobilization techniques to improve ankle dorsiflexion are commonly used in physiotherapy treatments. However, no studies have compared manipulative techniques of mobilization techniques in subjects with chronic ankle instability.
The aim of this study is to compare the effects of two mobilization techniques on ankle dorsiflexion in patients with chronic ankle instability.
| Condition | Intervention |
|---|---|
|
Chronic Instability of Joint |
Other: HVLA Other: MWM Other: placebo |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | The Effects of Two Techniques of Mobilization in the Improvement of Dorsiflexion on Chronic Instability Ankles. A Double Blind Randomized Controlled Trial |
Further study details as provided by CEU San Pablo University:
Primary Outcome Measures:
- Pre-intervention ankle dorsiflexion [ Time Frame: pre-intervention ] [ Designated as safety issue: Yes ]Ankle dorsiflexion is measured by the weight-bearing lunge method
- Inmediately post-intervention ankle dorsiflexion [ Time Frame: inmediately post-intervention ] [ Designated as safety issue: Yes ]Ankle dorsiflexion is measured by the weight-bearing lunge method
- ten minutes post-intervention ankle dorsiflexion [ Time Frame: ten minutes post-intervention ] [ Designated as safety issue: Yes ]Ankle dorsiflexion is measured by the weight-bearing lunge method
- 24 hr post-intervention ankle dorsiflexion [ Time Frame: 24 hr post-intervention ] [ Designated as safety issue: Yes ]Ankle dorsiflexion is measured by the weight-bearing lunge method
- 48 hr post-intervention ankle dorsiflexion [ Time Frame: 48 hr post-intervention ] [ Designated as safety issue: Yes ]Ankle dorsiflexion is measured by the weight-bearing lunge method
| Enrollment: | 52 |
| Study Start Date: | November 2010 |
| Study Completion Date: | November 2012 |
| Primary Completion Date: | December 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: HVLA
High velocity and low amplitude traction manipulation on the ankle joint
|
Other: HVLA
High velocity and low amplitude manipulation in traction of subtalar jonit
|
|
Experimental: MWM
Mobilization with movement on ankle joint as Mulligan
|
Other: MWM
Mobilization with movement as Mulligan for increase dorsiflexion of the ankle in weight bearing
|
|
Sham Comparator: placebo
Contact without therapeutic effect
|
Other: placebo
Manual contact during a period of time similar of teh other interventions
|
Eligibility| Ages Eligible for Study: | 15 Years to 40 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Subjects with chronic ankle instability
Exclusion Criteria:
- Acute or subacute ankle sprain.
- Recent lesions in lower extremities.
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Angel Luis Rodriguez, Professor at Physical Therapy Department, CEU San Pablo University |
| ClinicalTrials.gov Identifier: | NCT01618032 History of Changes |
| Other Study ID Numbers: | CEU-002 |
| Study First Received: | June 8, 2012 |
| Last Updated: | November 30, 2012 |
| Health Authority: | Spain: Ethics Committee |
Additional relevant MeSH terms:
|
Joint Instability Joint Diseases Musculoskeletal Diseases |
ClinicalTrials.gov processed this record on May 19, 2013