N/A
N=150
Direct Current Cathode and Anode Effects and Changes in Handgrip Strength. Evaluation Through a Dynamometer Test
Handgrip Strength
Bottom Line
View on ClinicalTrials.gov: NCT02884427 ↗Enrolled (actual)
150
Serious AEs
—
Results posted
Jul 2017
Primary outcome: Primary: Difference of Maximum Grip Strength — 03; 0; -02 Kilograms (Kg)
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Cathode stimulation (Device); Anode stimulation (Device); Placebo (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Quiropraxia y Equilibrio
- Primary completion
- Mar 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Difference of Maximum Grip Strength |
03; 0; -02 | — |
| SECONDARY Difference of Maximum Grip Strength for Males |
1; 0; 0.5 | — |
| SECONDARY Difference of Maximum Grip Strength for Females |
-0.3; -0.8; -0.8 | — |
Summary
The design aims to investigate the value of direct current, specifically the polar effects this has, and its influence on neuromuscular changes described in the literature. This research proposal seeks to assess the influence of application anode and cathode pole in muscle strength when testing handgrip dynamometry by healthy subjects. The study will evaluate changes in muscle strength when performing a manual dynamometer test in a group exposed to the application of cathode, another exposed to the application of anode, compared with a control that will not receive the intervention will be evaluated. Subsequently the investigators proceed to compare the maximum force obtained from the dynamometry test in each of groups and between the groups .
Eligibility Criteria
Inclusion Criteria
- Participants older than 18 years
- Do not manifest discomfort or pain when performing the handgrip.
Exclusion Criteria
- Skeletal muscle pathologies in hand, wrist or elbow in the last 6 months.
- Materials osteosynthesis or endoprosthesis in areas of application.
- Peripheral neurological pathologies as neuropraxias or nerve sections.
- Changes in the skin of the application areas, such as burns, wounds, scars.
- Apprehension or fear of the application of electrotherapy.
- No completion of the evaluation protocol / intervention, designed for study or abandonment.
Data sourced from ClinicalTrials.gov (NCT02884427). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.