Lateral Epicondylitis Clinical Trial
Official title:
Efficacy of Vitamin C Supplement Addiction vs. High-speed Spinal Manipulation to Routine Physiotherapy Treatment in Lateral Epicondylitis
A randomized clinical trial will be conducted. 130 subjects diagnosed with lateral epicondylitis will be studied. 3 intervention groups will be formed. Experimental group 1 will receive a 1000mg daily vitamin C supplement along with the usual practice of manual therapy and TENS. Group 2 will undergo high-speed vertebral manipulations along with manual therapy and TENS. In group 3 or control, manual therapy and transcutaneous electrotherapy (TENS) will be applied. All groups will receive the same manual therapy program and TENS, one session per week for 6 consecutive weeks. Data analysis: The data will be entered in the SPSS statistical package (version 21.0) for analysis). Statistical analysis will be performed with a 95% confidence interval, meaning that those whose P is <0.05 will be considered significant values.
The 130 subjects will be randomized into 3 groups: Experimental group 1 will receive a
supplement of vitamin C (ascorbic complex) of the Bonusan brand, a daily dose of 1000mg
should be consumed along with the usual practice of manual therapy and TENS. This group will
maintain the daily intake of vitamin C for the 6 weeks that the treatment lasts, they will be
informed of the possible side effects of adaptation to the supplement, such as, for example,
diarrhea since excess vitamin C, in the case if there is, it lodges in the large intestine,
which attracts fluid and produces osmotic diarrhea. This group will have direct communication
with the doctor who collaborates in this investigation for any situation, query or unwanted
symptom. Vitamin C has been used in other degenerative-type pathologies of collagen tissue
such as Achilles tendinopathies and supraspinatus musculature. The investigators have also
found references to the effect of vitamin C as pain treatment. Group 2 will undergo
high-speed vertebral manipulations along with manual therapy and TENS. Vertebral
manipulations would seek a reflexogenic effect through the sympathetic nerve pathway of the
lower cervical ganglion. The transcutaneous TENS-type stimulation is evidenced to have an
analgesic effect using self-adhesive patches placed longitudinally at the myo-junction.
tendon with a size of 50X50 mm, a frequency of 100 Hz and a pulse duration of 200μs for 25
minutes. Both the vertebral manipulation intervention and the TENS placement will be
performed by a professional health physiotherapist with 27 years of clinical experience in
the application of the aforementioned techniques.
In group 3 or control, manual therapy and transcutaneous electrotherapy (TENS) will be
applied. All groups will receive the same manual therapy program and TENS, one session per
week for 6 consecutive weeks.
All the aforementioned interventions will be included in a 45 minute session for the 3 groups
alike. They will be in charge of a highly qualified physiotherapist for all the therapies
when carrying out which expresses his consent for the study in. Said professional uses all
these therapies in consultation daily.
8 The aforementioned therapies can generate some adverse effects that the participants should
be aware of and that is reflected in the informed consent that they must complete before the
start of the evaluation and the interventions. In the first place, in the TENS, no
bibliography has been found that warns of any unwanted effect, which it can refer to is an
increase in skin tone under the patch due to the local effect and heat conduction of the
same. which should disappear within 30 minutes after application.
In high-speed vertebral manipulation in the cervical region, in 6% of cases,
post-manipulation dizziness may occur due to the local vascular change that occurs . The
vitamin C supplement can produce some type of heartburn diarrhea, especially in the first
days of taking, since this vitamin is absorbed in the intestine .
Alterations at the elbow can cause pain and functional limitation. To quantify these effects,
there are different measurement scales. The evaluation to quantify the pain will be carried
out with the numerical pain scale (0-10). The Disabilities of the Arm Shoulder and Hand
(DASH) questionnaire will be used to determine the functionality of the upper limb, the
Shoulder Pain and Disability Index SPADI will be used to assess shoulder function, Global
perception of change will also be evaluated, Global Rating of Change Scale (GROC) a 15-point
scale where -7 indicates much worse than before, 0 the same as before and +7 much better than
before . Finally, the pressure pain threshold (PDU) will be evaluated using a digital
algometer .
Measurement variables will be analyzed before treatment, after it, and at 3 and 6 months
after the last treatment session.
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