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The Effect of Vırtual Realıty Glasses on Heart Faılure Patıents

B

Bayburt University

Status

Not yet enrolling

Conditions

Heart Failure

Treatments

Behavioral: Virtual reality glasses
Behavioral: breathing exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT06838169
RCS2253148

Details and patient eligibility

About

Anxiety and sleep disorders are among the most common symptoms in heart failure patients. In addition to pharmacological methods for anxiety and sleep disorders, non-pharmacological methods can also be used. Among these, anxiety and sleep disorders can be prevented with virtual reality glasses aimed at distraction. This study will be conducted to evaluate the effect of breathing exercises performed with virtual reality glasses on anxiety, sleep quality, and respiratory parameters. The study will be conducted with a total of 45 patients, 15 virtual reality glasses + breathing exercises, 15 breathing exercises, and 15 controls. Those in the virtual reality glasses + breathing exercises group will perform breathing exercises with virtual reality glasses once a day for 7 days. Those in the breathing exercises group will perform only breathing exercises once a day for 7 days. Anxiety, sleep disorders, and respiratory parameters of the patients will be examined.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older,
  • Verbal communication,
  • Place and time oriented,
  • Without any psychiatric illness,
  • Patients diagnosed with HF with NYHA class III-IV symptoms,
  • Left ventricular ejection fraction ≥50% (LVEF-CF/HFpEF), between 40-49% (SEF-CF/HFmrEF), HF below 40% (DEF-CF/HFrEF),
  • High levels of natriuretic peptides (BNP>35 pg/mL and/or NTproBNP>125 pg/mL),
  • There is no deformity or diagnosis related to the musculoskeletal system that may prevent breathing exercise,
  • Chronic diseases such as hypertension (Stage 1 and 2 HT) and diabetes mellitus are stable and the treatment for these diagnoses has not been changed in the last month,
  • Who have not previously received respiratory exercise training and have not participated in a rehabilitation program,
  • Patients who volunteer to participate in the study will be included in the study

Exclusion criteria

  • Life signs are so abnormal as to preclude intervention,
  • Patients with migraine, vertigo, active nausea-vomiting, headache, dizziness will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

45 participants in 3 patient groups

Virtual reality glasses + breathing exercise app
Experimental group
Description:
Virtual reality glasses + breathing exercise app
Treatment:
Behavioral: breathing exercise
Behavioral: Virtual reality glasses
Breathing exercise practice
Active Comparator group
Description:
Breathing exercise practice
Treatment:
Behavioral: breathing exercise
Kontrol
No Intervention group
Description:
No application will be made

Trial contacts and locations

1

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Central trial contact

Özlem CEYHAN; Servet KALYONCUO

Data sourced from clinicaltrials.gov

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