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CompletedNCT03677453Updated Feb 3, 2021

Interactive Perioperative Teaching Platform (IPTP)

An interventional study of Interactive Perioperative Teaching Platform in Tonsillar Hypertrophy, Adenoid Hypertrophy and Cryptorchidism, sponsored by Vidya Raman. Completed at 1 site in United States. Open to participants aged Up to 18 Years. Per ClinicalTrials.gov, last updated 2021-02-03.

Sponsored by Vidya Raman · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
151
Allocation
Randomized
Ages
Up to 18 Years
Sex
All
01

Study summary

The proposed study will assess whether an interactive perioperative teaching platform (IPTP) provided to families of patients undergoing ambulatory pediatric surgery will reduce families' anxiety, and improve satisfaction and understanding, relative to current practice. The IPTP will educate patient families on the continuum of their child's surgical experience, from arriving at the hospital through registration, the operating room (OR), and the hospital floor. An active video format will be used to provide instructions for navigating the hospital; describe induction of anesthesia and the surgical procedure; and provide post-surgery and post-discharge instructions for pain management. A comparison cohort of patients undergoing surgery without access to the IPTP will be recruited to assess the benefits of the IPTP for improving metrics of family satisfaction, preoperative anxiety, and postoperative understanding of discharge instructions.

02

Conditions studied

  • Tonsillar Hypertrophy
  • Adenoid Hypertrophy
  • Cryptorchidism
  • Hypospadias
  • Hydrocele
03

In context

Cryptorchidism

40 studies on the registry are indexed under Cryptorchidism; 14 are open to participants now.

This study's enrollment of 151 is above the median of 70 across 26 interventional studies indexed under Cryptorchidism.

Browse Cryptorchidism studies →

Lead sponsor

Vidya Raman is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 18 Years
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

  • Children aged 0-18 years
  • Undergoing adenotonsillectomy or orchiopexy, hydrocele or hypospadias repair
  • Only patients booked for ambulatory surgery in the main operating room (OR)

Exclusion criteria

Exclusion Criteria:

  • Patients will be excluded if they have previously undergone surgery or require a translator
05

Study design

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

Study arms

  • Active comparator
    IPTP

    Patients will have access to the web-based interactive teaching tool.

    Other: Interactive Perioperative Teaching Platform

  • No intervention
    Non-IPTP

    Patients will not have access to the web-based interactive teaching tool.

Interventions

  • OtherInteractive Perioperative Teaching Platform

    An active video format will be used to provide instructions for navigating the hospital; describe induction of anesthesia and the surgical procedure; and provide post-surgery and post-discharge instructions for pain management.

    Also known as: IPTP

06

What researchers measure

Primary outcomes

  1. Patient family satisfaction

    Family satisfaction will be assessed by a member of the research team using an adaptation of the English version of the Leiden Perioperative Patient Satisfaction questionnaire (LPPSq) recommended for research on satisfaction with surgeries involving anesthesia. The English version assesses 4 domains of satisfaction: information provision, professional competence, patient-staff relationship, and service with a total of 24 questions on these topics. It is scored on a 1-5 Likert scale (from completely dissatisfied to completely satisfied).

    Time frame: Immediately prior to discharge

Secondary outcomes

  1. Anxiety level

    Anxiety will be measured using the short-form State-Trait Anxiety Inventory 10 with scores ranging from 6-24 (least to most anxious).

    Time frame: Baseline

07

Study locations

1 site
  • Nationwide Children's Hospital
    Columbus, Ohio 43205, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03677453
Lead sponsor
Vidya Raman
Responsible party
Vidya Raman (Clinical Associate Professor of Anesthesiology, Nationwide Children's Hospital) — Sponsor-investigator
First posted
Sep 19, 2018
Start date
Oct 10, 2018
Primary completion
Nov 30, 2020
Completion
Nov 30, 2020
Last update
Feb 3, 2021

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 completed, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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