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Skin Stretch Sensory Stimuli and TENS in Diabetic Neuropathy

R

Riphah International University

Status

Completed

Conditions

Diabetic Neuropathy

Treatments

Other: Skin stretch sensory stimuli
Other: Transcutaneous Electrical nerve stimulation
Other: Control Group

Study type

Interventional

Funder types

Other

Identifiers

NCT05250999
REC/Lhr/21/0213 Sobia Younas

Details and patient eligibility

About

The aim of the research was to find and compare the effects of skin stretch sensory stimuli and transcutaneous electrical nerve stimulation (TENS) on balance in diabetic neuropathy. Randomized controlled trial done at District Headquarter hospital Okara. The sample size was 46. The subjects were divided into 3 groups, 15 subjects in skin stretch sensory stimuli group, 15 subjects in TENS group and 16 subjects in control group. Study duration was of 6 month. Sampling technique applied was convenient non-probability sampling. Patients aged range from 45 to 80 years, having moderate peripheral neuropathy, and decrease sensations were included. Tools used in this study were Berg Balance scale and Toronto clinical neuropathy score system. Data was being analyzed through Spss 21.

Full description

Literature shows that various studies was done on diabetic patients for pain reduction, increase proprioception, improve muscle function and muscle recruitment by using kinesio tape and transcutaneous electrical nerve stimulation. There is particularly limited literature available on the effects of skin stretch sensory stimuli on balance in DN patients. Therefore, based on the literature study, there is crucial need for studying the effects of skin stretch sensory stimuli and TENS as a treatment approach. Thus, the current study will be an attempt to know the results of skin stretch sensory stimuli and TENS in DN patients.

Enrollment

46 patients

Sex

All

Ages

45 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • participants age ranged from 45 to 80 years' old
  • Both genders.
  • patients with moderate peripheral neuropathy 9-11 on Toronto Clinical Neuropathy Scoring system
  • HbA1c levels
  • peripheral neuropathic pain of >6 months' duration involving the lower extremities
  • history of diabetes treated with diet, oral hypoglycemic or insulin therapy
  • lower extremity symptoms such as muscle pain, decrease in sensations, Achilles tendon reflex, joint position sense of thumb
  • Sensory polyneuropathy because of type 2 diabetic diseases
  • Ability to walk household distance without assistance or with the use of assistive device such as cane.

Exclusion criteria

  • Considerable musculoskeletal deformity such as fracture, amputation, abnormality of ROM.
  • Previous history of knee or back surgery
  • Lower extremity arthritis that prevents standing
  • History of cardiovascular problems such as angina, MI
  • Symptomatic postural hypotension
  • Foot ulceration.
  • Skin problems such as rashes etc.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

46 participants in 3 patient groups

Skin stretch sensory stimuli
Experimental group
Description:
Skin stretch sensory stimuli along with conventional physiotherapy
Treatment:
Other: Skin stretch sensory stimuli
Transcutaneous Electrical Nerve Stimulation
Experimental group
Description:
Transcutaneous electrical nerve stimulation along with conventional physiotherapy
Treatment:
Other: Transcutaneous Electrical nerve stimulation
Control Group
Active Comparator group
Description:
Conventional physiotherapy included balance exercises, static exercise and dynamic exercise.
Treatment:
Other: Control Group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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