ClinicalTrials.gg
Not yet recruitingNCT07679659PEVAUpdated Jul 1, 2026

Effect of a Preoperative Educational Video on Anxiety Levels

An interventional study of QR Code Video and Tablet Video in Perioperative Anesthetic and Anxiety, sponsored by Aksaray University Training and Research Hospital. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-01.

Primary conditionAnxiety Disorders(the registry's first term)UnverifiedIs this wrong?The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it. No better condition is named, so the registry's term is kept.

Sponsored by Aksaray University Training and Research Hospital · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
360
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Preoperative anxiety is common among patients undergoing elective surgery and may negatively affect perioperative outcomes. This randomized controlled trial aims to evaluate the effectiveness of a short educational video in reducing preoperative anxiety. Participants will be assigned to one of three groups: a QR code-based video group, a tablet-based video group, or a control group receiving standard preoperative information. Anxiety levels will be assessed using the Amsterdam Preoperative Anxiety and Information Scale (APAIS). The secondary objective is to evaluate the utilization of QR code-based video education.

Read the detailed description

Preoperative anxiety is associated with adverse psychological and physiological responses and may negatively influence the perioperative experience. Educational interventions have been proposed as a practical strategy to improve patient understanding and reduce anxiety before surgery. Video-based education offers a standardized and accessible method for delivering information regarding anesthesia and surgical procedures.

Recent advances in digital health technologies have facilitated the use of mobile devices and QR code-based educational tools in routine clinical practice. However, evidence regarding the effectiveness of different modes of video delivery on preoperative anxiety remains limited.

This study will evaluate whether a brief educational video delivered through a QR code before the day of surgery or viewed on a tablet device immediately before surgery can reduce preoperative anxiety compared with standard care. In addition, the study will assess the feasibility and utilization of QR code-based patient education in the perioperative setting. The findings may contribute to the development of accessible and scalable patient education strategies aimed at improving the surgical experience and patient-centered care.

02

Conditions studied

  • Perioperative Anesthetic
  • Anxiety

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Keywords

  • Educational Video
  • Preoperative Anxiety
  • Patient Education
  • QR Code
03

In context

Anxiety Disorders Unverified

7,201 studies on the registry are indexed under Anxiety Disorders; 1,682 are open to participants now.

This study's planned enrollment of 360 is above the median of 80 across 6,057 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Aksaray University Training and Research Hospital is the lead sponsor of 25 studies on the registry; 2 are open to participants now.

Compared within Anxiety Disorders, the registry's first condition term, which may not be this study's main condition. Counted across the registry records on this site, refreshed daily. How we classify →

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Age 18 years or older.
  • Scheduled for elective surgery under anesthesia.
  • Able to understand Turkish.
  • Able to provide written .

Exclusion criteria

Exclusion Criteria:

  • Emergency surgery.
  • Visual or hearing impairment preventing video viewing.
  • Cognitive impairment.
  • Neurological or psychiatric disorders that may interfere with communication or completion of study questionnaires.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

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

Study arms

  • Experimental
    QR Code Video Group

    Participants will receive a QR code during the preoperative anesthesia clinic visit, allowing access to a brief educational video about anesthesia and surgery. Participants may view the video on their own devices before the day of surgery.

    Behavioral: QR Code Video

  • Experimental
    Tablet Video Group

    Participants will watch the same educational video on a tablet device in the preoperative waiting area immediately before surgery.

    Behavioral: Tablet Video

  • No intervention
    Control Group

    Participants will receive standard preoperative information and routine care without exposure to the educational video.

Interventions

  • BehavioralQR Code Video

    Participants received a QR code providing access to the standardized preoperative educational video. They were instructed to watch the video before surgery using their own smartphone or another internet-enabled device.

  • BehavioralTablet Video

    Participants viewed the standardized preoperative educational video on a tablet device provided by the study staff in the preoperative waiting area before surgery.

06

What researchers measure

Primary outcomes

  1. Amsterdam Preoperative Anxiety and Information Scale ( APAIS)

    The Amsterdam Preoperative Anxiety and Information Scale (APAIS) will be used to assess preoperative anxiety and information requirement. Scores range from 6 to 26, with higher scores indicating greater preoperative anxiety and information requirement (worse outcome).

    Time frame: On the day of surgery, immediately before induction of anesthesia

Secondary outcomes

  1. QR Code Utilization Rate

    The proportion of participants who accessed the educational video through the provided QR code before surgery.

    Time frame: From enrollment until immediately before anesthesia induction on the day of surgery, assessed up to 1 month

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Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Cetinkaya F, Kavuran E, Unal Aslan KS. Validity and reliability of the Amsterdam Preoperative Anxiety and Information Scale in the Turkish population. Turk J Med Sci. 2019 Feb 11;49(1):178-183. doi: 10.3906/sag-1806-84. PubMed 30764595 ↗
  • Moerman N, van Dam FS, Muller MJ, Oosting H. The Amsterdam Preoperative Anxiety and Information Scale (APAIS). Anesth Analg. 1996 Mar;82(3):445-51. doi: 10.1097/00000539-199603000-00002. PubMed 8623940 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07679659
Lead sponsor
Aksaray University Training and Research Hospital
Responsible party
Gülencan Yumuşak Ergin (MD, Aksaray University Training and Research Hospital) — Principal investigator
First posted
Jul 1, 2026
Start date
Jul 1, 2026 (estimated)
Primary completion
Nov 1, 2026 (estimated)
Completion
Dec 1, 2026 (estimated)
Last update
Jul 1, 2026

Study contacts

Gülencan Yumuşak Ergin, MD
Contact
gulencanyumusak@gmail.com
+905373587055
Tuğba Açıkgöz
Contact
gulencanyumusak@gmail.com
+905334318062
Gülencan Yumuşak Ergin, MD
principal investigator · Aksaray University Training and Research Hospital

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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