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The Effect of Local Cold Application on Hypertension

A

Ataturk University

Status

Unknown

Conditions

Hypertension

Treatments

Other: Experimental group
Other: Placebo group

Study type

Interventional

Funder types

Other

Identifiers

NCT04998526
yavuztez

Details and patient eligibility

About

This study will be conducted to evaluate the effect of local cold application to the nape of the neck on systolic blood pressure, diastolic blood pressure, heart rate, heart rate pressure and headache.

Full description

Aim: This study will be conducted to evaluate the effect of local cold application to the nape of the neck on systolic blood pressure, diastolic blood pressure, heart rate, heart rate pressure and headache.

Material and method: This study, which is planned as a randomized controlled and experimental study, will be conducted with type 2 (systolic blood pressure between 160 and 179 mmHg, diastolic blood pressure between 100 and 109 mmHg) essential hypertension patients who refer to Van Yüzüncü Yıl University Dursun Odabaş Medical Centre Emergency Service. The patients will be distributed as 24 in experimental group, 24 in placebo group and 24 in control group based on block randomization (gender and age) method and a total of 72 patients will be included. Patient information form, blood pressure and heart rate monitoring form and VAS pain scale will be used to collect study data. Patients in all groups will be measured in 90 minutes for a total of 8 times, as pre-test (pre-application) and post-test (minutes 3, 10, 15, 20, 30, 60 and 90). After routine medication therapy is given to all three groups, the cold gel pack which has been kept at least for four hours in the freezer will be applied to the nape of the patients in the experimental group, while gel pack at room temperature will be applied to the placebo group and no application will be made to the control group. Variance analysis, Friedman analysis, t test, Wilcoxon test and Kruskal Wallis analysis will be used in data assessment.

Enrollment

72 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 25 mg sublingual ACE inhibitor given as a treatment protocol,
  • No wound on the nape,
  • Does not develop cold intolerance,
  • Not taking any hypertension medication and pain medication in the last 6 hours,
  • Without heart diseases, peripheral arterial circulation disorders, sensory disorders and edema,
  • Not pregnant,
  • Agreeing to participate in the study,
  • Essential hypertension patients with systolic blood pressure 160 - 179 mmHg, diastolic blood pressure 100 - 109 mmHg.

Exclusion criteria

  • Developing cold intolerance,
  • Changes in the treatment regimen,
  • Panic attack, allergic reaction and any similar situation develops,
  • Those who want to withdraw from the research

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

72 participants in 3 patient groups, including a placebo group

Experimental group
Experimental group
Description:
After routine drug treatment is given to hypertension patients, the cold gel pack will be applied to the nape for 3 minutes.
Treatment:
Other: Experimental group
Placebo group
Placebo Comparator group
Description:
After routine drug therapy is given to hypertension patients, the gel pack kept at room temperature will be applied to the nape for 3 minutes.
Treatment:
Other: Placebo group
Control group
No Intervention group
Description:
Routine drug treatment will be given to hypertension patients and no application will be made.

Trial contacts and locations

1

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Central trial contact

YAVUZ ÜREN, PhD Student

Data sourced from clinicaltrials.gov

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