ClinicalTrials.gg
CompletedNCT07794709Updated Aug 31, 2026

Virtual Reality-Based Breathing Yoga Before Chest Tube Removal After Cardiac Surgery

An interventional study of Virtual Reality-Based Breathing Yoga in Anxiety, Chest Tube Removal and Pain After Surgery, sponsored by Sennur Kula Şahin. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-31.

Primary conditionPainRegistry: Anxiety DisordersReclassifiedWhy we changed it
Registry
Anxiety Disorders — the first condition term the registry derived for this study.
ClinicalTrials.gg
Pain
Why
  1. The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it.
  2. The study's listed conditions name Pain.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Sennur Kula Şahin · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 2 years after the study started (first participant enrolled Aug 2024, registered Aug 2026).

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Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 1,714 studies in Pain with a site in Turkey — 322 open to participants now, 372 under way, none of them phase 3. Pain · Turkey.

Enrollment
1,080th of 1,491
52 · median 70
Started
2024
with 289 others
No phase
1,449 of 1,714
260 open now
Registered
1,656th of 1,714
by date

Among the 1,714 studies in Pain with a site in Turkey, this one is the 1,080th largest by enrollment of the 1,491 interventional ones that give a count, is one of 290 that started in 2024, is one of 1,449 with no phase, and was the 1,656th registered.

Pain

10,060 studies on the registry are indexed under Pain; 1,651 are open to participants now.

Browse Pain studies →

Open to participants now

322 of the 1,714 studies in Pain with a site in Turkey are open now. Recruiting first, the newest first:

317 more — sign in →

All 322 open studies →

A study can be open while its sites in Turkey have not opened yet or have stopped. Only those recruiting at a site in Turkey →

Who these studies take

Of the 929 Pain studies recruiting now, 384 (41%) set no upper age limit and 434 (47%) stop at 75 or younger; 146 take children under 18; 222 take healthy volunteers.

This study: 18 Years to 70 Years · all sexes · healthy volunteers too.

The full table on the hub →

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02

Study summary

This randomized controlled trial was conducted to evaluate the effect of virtual reality-based breathing yoga applied before chest tube removal on pain and anxiety in patients after cardiac surgery. A total of 52 patients with chest tubes were randomly assigned to an intervention group (n=26) or a control group (n=26). Patients in the intervention group watched breathing yoga videos through virtual reality glasses for 15-20 minutes before chest tube removal, while patients in the control group received standard care. Pain was assessed using the Visual Analog Scale, and anxiety was assessed using the Spielberger State Anxiety Inventory. Pain and anxiety levels were evaluated before and after chest tube removal.

Read the detailed description

Chest tube removal after cardiac surgery may cause pain and anxiety. Non-pharmacological approaches such as virtual reality and breathing-based relaxation techniques may help improve patient comfort during invasive procedures.

This prospective, parallel, two-arm, single-center randomized controlled trial evaluated the effect of virtual reality-based breathing yoga before chest tube removal in patients who had undergone cardiac surgery. Eligible participants were randomly allocated in a 1:1 ratio to the intervention or control group.

Participants in the intervention group received a 15-20-minute virtual reality-based breathing yoga intervention before chest tube removal in addition to standard care. Participants in the control group received standard care without the virtual reality intervention. Pain and state anxiety were assessed before and after chest tube removal using the Visual Analog Scale and the Spielberger State Anxiety Inventory, respectively.

03

Conditions studied

  • Anxiety
  • Chest Tube Removal
  • Pain After Surgery

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Keywords

  • Virtual Reality
  • Breathing Yoga
  • Cardiac Surgery
  • Pain
  • Anxiety
  • Nonpharmacological Intervention
04

In context

Pain Reclassified

10,060 studies on the registry are indexed under Pain; 1,651 are open to participants now.

This study's enrollment of 52 is below the median of 66 across 8,497 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Sennur Kula Şahin is the lead sponsor of 4 studies on the registry; none are open to participants now.

Compared within Pain, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Anxiety Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →

05

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18-70 years
  • Underwent coronary artery bypass grafting or valve surgery
  • Willing to participate in the study
  • Mobilized and extubated on the second postoperative day
  • Able to communicate without cognitive, sensory, or verbal impairment
  • No diagnosed psychiatric disorder
  • No vertigo
  • No diagnosis of hypertension and not receiving antihypertensive treatment
  • Not receiving sedative or anxiolytic medication
  • No major intraoperative or postoperative complications, such as severe bleeding, nausea, or vomiting

Exclusion criteria

Exclusion Criteria:

- Remained intubated on the second postoperative day

06

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
52 participants (actual)

Study arms

  • Experimental
    1

    Virtual Reality-Based Breathing Yoga

    Behavioral: Virtual Reality-Based Breathing Yoga

  • No intervention
    2

    Participants received standard care before chest tube removal without the virtual reality-based breathing yoga intervention.

Interventions

  • BehavioralVirtual Reality-Based Breathing Yoga

    Participants watched breathing yoga videos through virtual reality glasses for 15-20 minutes before chest tube removal. The intervention was provided in addition to standard postoperative care.

07

What researchers measure

Primary outcomes

  1. Change in State Anxiety Level

    State anxiety was assessed using the Spielberger State-Trait Anxiety Inventory-State subscale (STAI-I). The scale consists of 20 items and yields a total score ranging from 20 to 80, with higher scores indicating higher levels of state anxiety.

    Time frame: 30 minutes before chest tube removal and 15 minutes after chest tube removal

Secondary outcomes

  1. Change in Pain Intensity

    Pain intensity was assessed using the Visual Analog Scale (VAS). Participants indicated their perceived pain intensity on a line anchored from "no pain" to "very severe pain," with higher values indicating greater pain intensity.

    Time frame: 30 minutes before chest tube removal and 15 minutes after chest tube removal

08

Study locations

1 site
  • Prof. Dr. Cemil Tascioglu City Hospital
    Istanbul, Istanbul 34010, Turkey (Türkiye)
09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2024 to primary completion in Jan 2025, 4 months.

Of 3,734 non-industry interventional studies with no phase under Pain, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 23. This study's 4 months is below that.

Counting every sponsor, half of 3,833 studies reached it within 10 months; a quarter within 4 and three quarters within 23.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 26, 2026
First posted
Aug 31, 2026
StartActual
Aug 10, 2024
Primary completionActual
Jan 1, 2025
CompletionActual
Jan 1, 2025
Last update
Aug 31, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT07794709
Lead sponsor
Sennur Kula Şahin
Responsible party
Sennur Kula Şahin (Assosciate Prof, Istinye University) — Sponsor-investigator
First posted
Aug 31, 2026
Start date
Aug 10, 2024
Primary completion
Jan 1, 2025
Completion
Jan 1, 2025
Last update
Aug 31, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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