The Effect of Virtual Forest Bathing on Bariatric Surgery Patients

NCT ID: NCT07152054

Last Updated: 2025-09-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-25

Study Completion Date

2026-08-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will be conducted at the General Surgery Clinic of City Hospital in Erzurum between August 2025 and April 2026 using a randomized controlled experimental design. In the power analysis, it was determined that the sample of the study should be 70 patients in total, 35 patients in each group, with a medium effect size of 0.5% according to Cohen (42), a margin of error of 0.05%, a confidence interval of 0.95%, and a 95% universe representation power. Patients will be assigned to either the experimental or control groups using a random number generator using a two-block randomization method (random.org). Given that exposure to nature through virtual reality increases physiological arousal and promotes positive mood, the study aimed to evaluate the effects of virtual forest bathing on pre- and postoperative pain, anxiety, fear, sleep, vital signs, and cortisol levels in patients undergoing bariatric surgery.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Bariatric surgery is considered an effective method for the treatment of obesity and is increasingly being performed worldwide. While bariatric surgery is an effective method for weight loss and control, the physiological changes caused by excess weight caused by surgical and anesthesia procedures can lead to postoperative complications. Before and after bariatric surgery, uncertainty about the surgical process, concerns about the surgical procedure and anesthesia procedures, and postoperative lifestyle changes and concerns about potential complications all contribute to an increased surgical stress response in obese individuals. Integrating non-pharmacological interventions into the treatment process, rather than focusing solely on pharmacological methods, is crucial. These approaches can be effective in alleviating the physical and psychological symptoms associated with surgery; they can support the recovery process by reducing anxiety and improving sleep quality. Techniques based on distraction, such as virtual reality, music therapy, and breathing exercises, do not produce any side effects, unlike pharmacological agents. These methods also help patients maintain basic physiological parameters such as blood pressure, respiration, and pulse rate, while also contributing to increased comfort and satisfaction. One of these innovative approaches is forest bathing, also known as "Shinrin-yoku," meaning "immersing in the forest atmosphere." Forest bathing utilizes the healing effects of forests to improve health and prevent disease through forest walks. Forest atmospheres are known to contain numerous healing factors that play an important role in the prevention and treatment of health problems through sensory input. There is evidence that forest bathing can help individuals regain attention and foster more positive emotions. Forest environments have positive effects on the cardiovascular system, nervous system, endocrine system, immune system, and mental health. This study was designed considering the need for evidence regarding the pre- and postoperative use of virtual forest bathing in the context of nursing care. It is believed that virtual forest bathing may have positive effects on pain, anxiety, fear, sleep patterns, cortisol, and vital signs in patients undergoing bariatric surgery during the pre- and postoperative periods. Virtual forest bathing has demonstrated successful results in various areas and with different patient groups for reducing stress and anxiety. However, there are limited studies specifically related to bariatric surgery, both in our country and elsewhere. Some studies abroad have shown that such psychological support methods have positive effects on surgical stress, but the number of studies conducted in this area in our country is quite limited. Therefore, this study is valuable in providing scientific data to healthcare professionals in our country. As experimental research on forest bathing intensifies, medical and healthcare professionals have focused on the forest's ability to boost immunity and reduce stress. They have concluded that even short-term forest bathing can help strengthen the body's immune system and improve mood. Implementing holistic, non-pharmacological interventions for patients experiencing both physical and psychological challenges before and after bariatric surgery is crucial. Virtual reality-based nature interventions are considered among the innovative and effective approaches that can be integrated into nursing care during this process. In this context, the study aimed to evaluate the effects of virtual forest bathing on pain, anxiety, fear, sleep patterns, vital signs, and cortisol in patients undergoing bariatric surgery before and after surgery.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Bariatric Surgery Virtual Reality Anxiety

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Experimental: Virtual Forest Bathing

Patients in the experimental group will undergo the routine surgical procedure implemented in the hospital, and their evaluations will be carried out using the predetermined questionnaires. In addition, they will receive a virtual forest bathing intervention on the evening prior to surgery and on the first postoperative day. On the day of admission for bariatric surgery, the researcher will administer, face-to-face, the Personal Information Form, Surgical Fear Questionnaire, Richard-Campbell Sleep Questionnaire, Visual Analog Scale (VAS) for pain assessment, State-Trait Anxiety Inventory, and the parameter recording form. Following the virtual forest bathing sessions conducted on the evening before surgery and on the first postoperative day, the Surgical Fear Questionnaire, Richard-Campbell Sleep Questionnaire, Visual Analog Scale (VAS), State-Trait Anxiety Inventory, and parameter recording form will be completed again.

Group Type EXPERIMENTAL

virtual forest bathing

Intervention Type DEVICE

Virtual reality (VR) is an advanced computer technology and a novel technique used in healthcare to alleviate pain and provide patient comfort. It enables individuals to interact with a 360-degree virtual environment through a headset device. It has been observed that painful or emotionally stressful stimuli from the external world are diminished within the VR environment, with the individual's attention redirected and focused on this immersive setting.

In our study, a 20-minute VR video will be used, providing the sensation of walking through a calming 360-degree virtual forest environment accompanied by natural sounds, viewed through VR headsets. Unlike some commercially available VR headsets, the Oculus Quest 2 model will be utilized, as it serves as both the computer and display system, eliminating the need for a smartphone. This device is preferred for its ability to deliver high-quality video without interruptions that might negatively affect the VR experience.

After explaining

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

virtual forest bathing

Virtual reality (VR) is an advanced computer technology and a novel technique used in healthcare to alleviate pain and provide patient comfort. It enables individuals to interact with a 360-degree virtual environment through a headset device. It has been observed that painful or emotionally stressful stimuli from the external world are diminished within the VR environment, with the individual's attention redirected and focused on this immersive setting.

In our study, a 20-minute VR video will be used, providing the sensation of walking through a calming 360-degree virtual forest environment accompanied by natural sounds, viewed through VR headsets. Unlike some commercially available VR headsets, the Oculus Quest 2 model will be utilized, as it serves as both the computer and display system, eliminating the need for a smartphone. This device is preferred for its ability to deliver high-quality video without interruptions that might negatively affect the VR experience.

After explaining

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Willingness to participate in the study
* Ability to communicate verbally
* Absence of any psychiatric disorder
* Undergoing bariatric surgery
* No prior experience with virtual forest bathing

Exclusion Criteria

* Inability to establish communication
* Presence of major hearing or visual impairment
* Presence of any condition that may affect decision-making ability (e.g., psychological disorders, dementia)
* Use of medications that may affect cognitive status (e.g., sedatives, antipsychotics)
* Patients who report having previously experienced virtual forest bathing will be excluded from the sample
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ataturk University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Muazzez Merve TORAMAN

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Muazzez Merve TORAMAN

Role: PRINCIPAL_INVESTIGATOR

Atatürk Üniversity

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Muazzez Merve TORAMAN

Role: CONTACT

05548307383

Zeynep KARAMAN ÖZLÜ, Prof. Dr.

Role: CONTACT

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Muazzez TORAMAN

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Health Tourism in Bariatric Surgery
NCT06694831 ACTIVE_NOT_RECRUITING
Opioid-Free Versus Opioid-Based Anesthesia in Bariatric
NCT07105839 NOT_YET_RECRUITING PHASE4
Vestibular Function in Obesity
NCT07033221 RECRUITING