NCT06941207

Brief Summary

The research will be conducted to evaluate the effects of Virtual Reality-Based Video and Benson Relaxation Exercise Applied to Palliative Care Providers on Sleep Quality, Fitness and General Well-Being. In the Palliative Care Center; The palliative patient group will be comprised of individuals aged 18 and over who provide care. The population of the research consists of 210 people. Individuals will be distributed to the virtual reality video experimental group (30), Benson relaxation exercise experimental group (30) and control (30) groups by simple randomization method. Personal Information Form, Sleep Quality Index, Subjective Wellness Scale and General Well-Being Scale will be used to collect research data. Personal information form, Sleep Quality Index, Subjective Well-Being Scale and General Well-Being Scale will be administered to the caregivers in both the experimental group and the control group by the researcher using face-to-face interview technique (pre-test). The caregivers, the first group in the experimental group, will be shown a total of 8 sessions of virtual reality-based videos (nature, forest walks and city tours, etc.) for an average of 30 minutes, twice a week for 4 weeks. The caregivers, who are the second group in the experimental group, will have a total of 8 sessions of Benson relaxation exercises for 20-25 minutes, twice a week for 4 weeks. No intervention will be made to the caregivers in the control group. At the end of the sessions, Sleep Quality Index, Subjective Well-Being Scale and General Well-Being Scale (post-test) will be applied to the experimental and control groups. The basic question it aims to answer is: Do virtual reality-based video and BENSON relaxation exercises applied to palliative care givers affect sleep quality, vitality and general well-being?

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 10, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

April 23, 2025

Completed
8 days until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
Last Updated

April 23, 2025

Status Verified

April 1, 2025

Enrollment Period

8 months

First QC Date

April 10, 2025

Last Update Submit

April 19, 2025

Conditions

Keywords

palliative carebenson relaxation exercisevirtual realitysleep quality

Outcome Measures

Primary Outcomes (3)

  • Pittsburgh Sleep Quality Index

    PSQI, developed by Buysse et al. (1989) and validated and reliable in Turkish by Ağargün (1996), is a self-report-based assessment tool that provides information about sleep quality and the type and severity of sleep disorders in the last month.

    1 month

  • subjective fitness scale

    Subjective Wellness Scale (SWS) is a scale developed by Ryan and Frederick in 1997. The adaptation of the scale to Turkish and its validity and reliability studies were conducted by Uysal et al. (2014). ESS is a self-report measuring tool consisting of 7 items and on a 7-point Likert scale (1 strongly disagree - 7 strongly agree).

    1 month

  • General Well-Being Scale Short Form

    The General Well-Being Scale, developed by Longo et al. (2018) and adapted into Turkish by Odacı et al. (2021), consists of 14 items that aim to measure the person's affect and satisfaction level with his life. Within the scope of the validity studies of the scale, confirmatory factor analysis, correlational analysis and independent samples t test were performed. According to the results of the factor analysis, it was confirmed that the scale had a single-factor structure. As a result of the criterion-related validity analysis, a significant positive relationship was detected between the participants' general well-being levels and positive affect, their life satisfaction and their needs satisfaction; A significant negative relationship was detected between negative emotions and negative emotions.

    1 month

Study Arms (3)

virtual reality video viewing group

EXPERIMENTAL

The first group in the experimental group, the virtual reality video group, caregivers, will be shown a total of 8 sessions of virtual reality-based videos (nature, forest walk and city tour, etc.) for an average of 30 minutes, twice a week for 4 weeks.

Behavioral: virtual reality video viewing group

The group to which Benson relaxation exercise will be applied

EXPERIMENTAL

The second group in the experimental group, the caregivers, will have a total of 8 sessions of Benson relaxation exercises for 20-25 minutes, twice a week for 4 weeks.

Behavioral: benson relaxation exercise group

control group

NO INTERVENTION

No intervention will be made to the caregivers in the control group.

Interventions

The caregivers, the first group in the experimental group, will be shown a total of 8 sessions of virtual reality-based videos (nature, forest walks and city tours, etc.) for an average of 30 minutes, twice a week for 4 weeks.

virtual reality video viewing group

The second group in the experimental group, the caregivers, will have a total of 8 sessions of Benson relaxation exercises for 20-25 minutes, twice a week for 4 weeks.

The group to which Benson relaxation exercise will be applied

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being literate,
  • Being over the age of 18,
  • Having sufficient communication skills to answer oral and written questions and follow instructions,
  • Being a palliative care provider for at least 6 months
  • Does not have visual/verbal/auditory communication difficulties that would prevent understanding the information presented and expressing the answers correctly,
  • Being a caregiver who can communicate in Turkish
  • Not having severe vision problems

You may not qualify if:

  • Sleep Quality Index score of 4 or less
  • Being over 65 years old
  • Palliative care providers who leave the study voluntarily
  • Presence of chronic disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Sleep Initiation and Maintenance Disorders

Condition Hierarchy (Ancestors)

Sleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SEQUENTIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD student

Study Record Dates

First Submitted

April 10, 2025

First Posted

April 23, 2025

Study Start

May 1, 2025

Primary Completion

January 1, 2026

Study Completion

January 1, 2026

Last Updated

April 23, 2025

Record last verified: 2025-04