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Effect of Acupressure Applied Before Cystectomy on Preoperative Anxiety Level

M

Mersin University

Status

Completed

Conditions

Hemodynamic Instability
Anxiety

Treatments

Other: Acupressure
Other: Placebo acupressure

Study type

Interventional

Funder types

Other

Identifiers

NCT05325307
Mersin Univ

Details and patient eligibility

About

This randomized controlled study evaluates the effect of acupressure application on the anxiety level patients undergoing cystectomy surgery. The hypothesis of this study is that acupressure reduces anxiety levels and stabilizes hemodynamic parameters.

Full description

In the study, 60 patients will randomly assigned to acupressure and placebo acupressure groups. To the acupressure group (n = 30), an average of 15 minutes will be applied to the HT7 (heart), LI4 (liver) and EX-NH3 (the point between the two eyes). In the placebo acupressure group (n = 30), the points 1.5 cm away from the HT7, LI4, and EX-NH3 points will be applied for an average of 15 minutes.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Agreeing to participate in the research (signing the Informed Consent Form),
  • Conscious and cooperative
  • Speaks and understands Turkish,
  • 18-65 years old,
  • Before surgery,
  • Stable general condition,
  • No sensitivity in the area where acupressure/placebo acupressure will be applied,
  • 15 July 2022 - 15 July 2023 hospitalized in the urology clinic,
  • No active COVID-19 infection,
  • Patients without any psychiatric diagnosis will be included.

Exclusion criteria

  • Those who do not agree to participate in the research (who do not sign the Informed Consent Form)
  • Conscious and uncooperative,
  • Not speaking or understanding Turkish,
  • Not between the ages of 18-65,
  • No surgical intervention planned,
  • The planned emergency surgical intervention,
  • Unstable general condition,
  • Sensitivity in the area where acupressure/placebo acupressure will be applied,
  • Active COVID-19 infection,
  • 15 July 2022 - 15 July 2023 who did not stay in the urology clinic,
  • Patients with current psychiatric diagnosis will not be included in the study.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups, including a placebo group

Acupressure Group (experimental)
Experimental group
Description:
The experimental group will be given acupressure.
Treatment:
Other: Acupressure
Placebo Acupressure Group (control)
Placebo Comparator group
Description:
The placebo group will be given placebo acupressure
Treatment:
Other: Placebo acupressure

Trial contacts and locations

1

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Central trial contact

Tugba CAM YANIK, PhD

Data sourced from clinicaltrials.gov

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