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Completed

NCT Number: NCT07413289

Pediatric Recovery Delirium in Pediatric Patients Undergoing Surgery

The primary aim of this observational study is to evaluate the effect of playing a mother's voice to a child while the patient is being awakened from anesthesia on postoperative delirium. For this purpose, a recording of the mother's voice will be prepared before surgery. In this recording, the mother will reassure the child that they are safe and encourage them to remain calm. This recording will then be played to the patient during the awakening phase from anesthesia. The frequency of postoperative delirium in participants who were awakened by the voice recording will be compared with that of the patient group who were awakened without the voice recording.

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Key information

About this study

In this study, mothers' anxiety levels will be measured and recorded using the STAI 1 and 2 questionnaires. Children's postoperative anxiety will be recorded using the modified Yale questionnaire and the PAED. Additionally, the FLACC scale will be used to record information in postoperative children.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pediatric patients who will undergo adenotonsillectomy surgery

Exclusion criteria

  • children whose mother or child has hearing or speech impairments and chronic/genetic diseases

Treatment and study plan

Primary outcomes

  1. postoperative delirium

    Time frame: about a month and a half

    The primary aim of this study is to evaluate the effect of playing a mother's voice to a child while the patient is being awakened from anesthesia on postoperative delirium. To assess this effect, participants will be administered the Modified Yale Preoperative Anxiety Scale, and in the postoperative period, the PAED and FLACC scales will also be applied.

Secondary outcomes

  1. The mother's current and sustained anxiety levels.

    Time frame: 1 and a half months

    The mother will be asked to complete STAI TX 1 and STAI TX 2 forms, respectively, to assess her anxiety levels in both her immediate and normal daily life. The aim is to evaluate the relationship between the mother's anxiety level and the patient's frequency of delirium.

Sponsors and collaborators

Lead sponsor

Enes Celik

Other

Registry information

Official study title

The Effect Of Recorded Maternal Voice On Pediatric Recovery Delirium In Pediatric Patients Undergoing Adenotonsillectomy Surgery

Acronym: Delirium

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 17, 2026
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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