An interventional study of Family Video.Participants watched a five-minute video prepared by their family members twice daily on the second and third days of intensive care. in Anxiety, Agitation and Pain, sponsored by Sennur Kula Şahin. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-01.
Sponsored by Sennur Kula Şahin · Not applicable, Interventional, and Supportive care
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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.
Among the 1,714 studies in Pain with a site in Turkey, this one is the 677th 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.
10,060 studies on the registry are indexed under Pain; 1,651 are open to participants now.
Browse Pain studies →322 of the 1,714 studies in Pain with a site in Turkey are open now. Recruiting first, the newest first:
Mersin University · Sites in Turkey
Ages 18+
Artvin Coruh University · Sites in Turkey
Ages 6–12
Mersin University · Sites in Turkey
Ages 18+
Bahçeşehir University · Sites in Turkey
Ages 45–65
Istanbul University · Sites in Turkey
Ages 1–12
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 →
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 80 Years · all sexes · no healthy volunteers.
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1,714 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 1 1 · Phase 2 3 · Phase 3 6 · Phase 4 34
First in 2006; this study’s year is marked. 290 started in 2024.
By drug class, each counting the studies that test any of its medicines:
This study's enrollment of 72 is close to the median of 66 across 8,497 interventional studies indexed under Pain.
Median enrollment 70 across the 1,491 interventional studies, 84 across the 223 observational. Of the 1,270 that completed or were terminated, 7 (1%) have results posted.
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4 of 1,714 have an industry lead sponsor. The 10 most frequent:
Sennur Kula Şahin is the lead sponsor of 4 studies on the registry; none are open to participants now.
Sennur Kula Şahin has 2 studies filed under Pain — fewer than ten, so there is no comparison to draw.
85 of the studies in Pain with a site in Turkey that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT07707726Ankara City Hospital BilkentVirtual Reality in Ingrown Toenail Surgery | 2026-11-15 |
| NCT07846098Cumhuriyet UniversityComparison of Intraosseous Anesthesia and Inferior Alveolar Nerve Block for Primary Mandibular Molars | 2026-11-20 |
| NCT07404163Tarsus UniversityWalkway Used in Postoperative Mobilization | 2026-11-30 |
| NCT07915804Istanbul UniversityPerfusion Index for Postoperative Pain Assessment in Pediatric Adenotonsillectomy | 2026-11-30 |
| NCT07892196Antalya Training and Research HospitalDoes Chronic Pain Change Over Time in Children With Duchenne Muscular Dystrophy? | 2026-11-30 |
Add all 85 to your calendar (.ics) → With an account.
Among the 1,714 studies in Pain with a site in Turkey, from their registry updates:
This tab as a report to print or save as PDF → With an account.
This randomized controlled trial was conducted to evaluate the effects of family videos and virtual reality-based nature videos on anxiety, agitation, pain, and vital signs in adult intensive care unit patients. A total of 72 participants were randomly assigned to three parallel groups: a family video group (n=24), a family video plus virtual reality-based nature video group (n=24), and a standard care control group (n=24). Anxiety, agitation, pain, and vital signs were assessed before and after the interventions during the second and third days of intensive care.
Intensive care unit patients may experience psychological and physiological problems such as anxiety, agitation, and pain because of the stressful and isolating nature of the intensive care environment. This randomized controlled trial evaluated family-based visual support and virtual reality-based nature videos as non-pharmacological supportive interventions in adult intensive care unit patients.
Participants were randomly assigned to one of three parallel groups. In the first intervention group, participants watched five-minute family videos twice daily. In the second intervention group, participants watched five-minute family videos twice daily and additionally viewed nature-themed videos using a virtual reality headset once daily for approximately 15-20 minutes. Participants in the control group received standard treatment and nursing care without a study-specific video or virtual reality intervention.
The interventions and assessments were performed on the second and third days of intensive care after the patients' clinical condition had been evaluated and approved by a physician. Anxiety, agitation, and pain were assessed immediately before and after the interventions. Vital signs were obtained from routine clinical monitoring records. During virtual reality sessions, the researcher remained with the participant and monitored for possible adverse effects such as dizziness
10,060 studies on the registry are indexed under Pain; 1,651 are open to participants now.
This study's enrollment of 72 is close to the median of 66 across 8,497 interventional studies indexed under Pain.
Browse Pain studies →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 →
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Aged 18-80 years
Exclusion Criteria:
Visual or hearing impairment
Family Video Intervention:Participants watched five-minute family videos twice daily on the second and third days of intensive care. Anxiety, agitation, pain, and vital signs were assessed immediately before and after the intervention.
Behavioral: Family Video.Participants watched a five-minute video prepared by their family members twice daily on the second and third days of intensive care.
Family Video Plus Virtual Reality Group. Participants watched five-minute family videos twice daily and additionally viewed nature-themed videos using a virtual reality headset once daily for 15-20 minutes on the second and third days of intensive care. Anxiety, agitation, pain, and vital signs were assessed before and after the interventions.
Behavioral: Family Video.Participants watched a five-minute video prepared by their family members twice daily on the second and third days of intensive care.
Standard Care Control Group. Participants received standard treatment and nursing care without a study-specific family video or virtual reality intervention. Outcomes were assessed at the same times and frequency as in the intervention groups.
Participants viewed nature-themed video content using a virtual reality headset for approximately 15-20 minutes once daily on the second and third days of intensive care. The researcher remained with participants during the session and monitored for possible adverse effects.
State Anxiety Level
State anxiety was assessed using the State-Trait Anxiety Inventory-State (STAI-I). The scale consists of 20 items, with total scores ranging from 20 to 80. Higher scores indicate higher levels of state anxiety.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Agitation-Sedation Level
Agitation and sedation were assessed using the Richmond Agitation-Sedation Scale (RASS), which ranges from -5 to +4. Positive scores indicate increasing levels of agitation, 0 indicates an alert and calm state, and negative scores indicate increasing levels of sedation.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Pain Intensity
Pain intensity was assessed using a Numerical Pain Rating Scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates the most severe pain.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Heart Rate
Description: Heart rate was recorded before and after the intervention sessions. Time Frame: Immediately before and after the intervention sessions on intensive care unit days 2
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Respiratory Rate
Respiratory rate was recorded before and after the intervention sessions.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Systolic Blood Pressure
Systolic blood pressure was recorded before and after the intervention sessions.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Diastolic Blood Pressure
Diastolic blood pressure was recorded before and after the intervention sessions.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Body Temperature
Body temperature was recorded before and after the intervention sessions.
Time frame: Immediately before and after the intervention sessions on intensive care unit days 2 and 3.
Plan to share: No
No publications or documents are linked to this record.
Ran from Oct 2024 to primary completion in Mar 2025, 5 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 5 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.
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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Sennur Kula Şahin