ClinicalTrials.gg
Enrolling by invitationNCT07740759Updated Aug 3, 2026

Impact of Educational Videos on Pre-operative Anxiety

An interventional study of educational video in Endometriosis, Fibroids and Adenomyosis, sponsored by UConn Health. Enrolling by invitation at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-03.

Sponsored by UConn Health · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study summary

The goal of this clinical trial is to learn if educational videos can reduce pre-operative anxiety in patients undergoing minimally invasive gynecologic surgery. The main question it aims to answer are:

do patient education videos decrease preoperative anxiety? do patient education videos increase patient preparedness for surgery? Researchers will compare the group who watched the videos preoperatively to the group who only underwent the usual counseling at the preoperative visit to see if the results of a survey that measures anxiety and preparedness differ.

Participants will be randomly assigned to one of two groups: one group that will be asked to watch the educational videos and one group that will not. All participants will attend their pre-operative appointment as usual and complete a survey afterwards.

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Conditions studied

  • Endometriosis
  • Fibroids
  • Adenomyosis
  • Pelvic Pain
  • Abnormal Uterine Bleeding
  • Adnexal Mass
  • Minimally Invasive Gynecologic Surgery
  • Hysterectomy
  • Myomectomy
  • Ovarian Cystectomy
  • Adnexal Surgery

Keywords

  • minimally invasive gynecologic surgery
  • pre-operative anxiety
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In context

Endometriosis

920 studies on the registry are indexed under Endometriosis; 266 are open to participants now.

This study's planned enrollment of 60 is below the median of 67 across 540 interventional studies indexed under Endometriosis.

Browse Endometriosis studies →

Lead sponsor

UConn Health is the lead sponsor of 187 studies on the registry; 18 are open to participants now.

Of its 10 completed or terminated interventional studies of FDA-regulated products, 7 (70%) have results posted.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
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

  • English speaking patients over the age of 18 who plan to undergo any of the following laparoscopic surgeries, which includes robotic-assisted laparoscopy, with a MIGS provider: diagnostic laparoscopy, laparoscopic endometriosis excision, adnexal surgery, laparoscopic myomectomy, total laparoscopic hysterectomy
  • Concomitant procedures permitted (such as bowel resection for endometriosis, hysteroscopy, dilation and curettage, cystoscopy, etc.)

Exclusion criteria

Exclusion Criteria:

  • Pregnant patients
  • Incarcerated patients
  • Patients under the age of 18
05

Study design

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

Study arms

  • Experimental
    Video group

    This group will be provided the educational videos to watch before their preoperative appointment.

    Other: educational video

  • No intervention
    Usual care group

    This group will not be sent the educational videos before their preoperative appointment.

Interventions

  • Othereducational video

    The videos provide an overview of the following topics: preoperative instructions, female pelvic anatomy, positioning during surgery, the uterine manipulator device, pelvic laparoscopy, total hysterectomy, and postoperative instructions.

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What researchers measure

Primary outcomes

  1. Preoperative anxiety as measured by the State Trait Anxiety Inventory (STAI)

    The STAI will be used to survey the anxiety patients feel in relation to their upcoming surgery. An STAI score of ≥ 40 has been used to define clinical anxiety in the literature, so this will be the threshold to define clinically significant pre-operative anxiety. STAI scores will be compared between groups using linear regression models, both unadjusted and adjusted for any unbalanced baseline covariates.

    Time frame: once, at the preoperative appointment

Secondary outcomes

  1. Preoperative patient preparedness

    Preparedness will be measured by a patient preparedness questionnaire (PPQ). Preparedness will be determined by answering "strongly agree" to the last question on the PPQ ("Overall, I feel prepared for my upcoming surgery"). Preparedness will be analyzed using logistic regression models, also with and without covariate adjustment.

    Time frame: Once, at the preoperative appointment

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Study locations

1 site
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References and documents

Publications

  • Kenton K, Pham T, Mueller E, Brubaker L. Patient preparedness: an important predictor of surgical outcome. Am J Obstet Gynecol. 2007 Dec;197(6):654.e1-6. doi: 10.1016/j.ajog.2007.08.059. PubMed 18060968 ↗
  • Sassani JC, Grosse PJ, Kunkle L, Baranski L, Ackenbom MF. Patient Preparedness for Pelvic Organ Prolapse Surgery: A Randomized Equivalence Trial of Preoperative Counseling. Female Pelvic Med Reconstr Surg. 2021 Dec 1;27(12):719-725. doi: 10.1097/SPV.0000000000001049. PubMed 33787563 ↗
  • Wilson CJ, Mitchelson AJ, Tzeng TH, El-Othmani MM, Saleh J, Vasdev S, LaMontagne HJ, Saleh KJ. Caring for the surgically anxious patient: a review of the interventions and a guide to optimizing surgical outcomes. Am J Surg. 2016 Jul;212(1):151-9. doi: 10.1016/j.amjsurg.2015.03.023. Epub 2015 Jun 2. PubMed 26138522 ↗

Individual participant data

Plan to share: No

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Updates

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

Key details

Study ID
NCT07740759
Lead sponsor
UConn Health
Responsible party
Alexis Newmark (Assistant Professor of Obstetrics and Gynecology, UConn Health) — Principal investigator
First posted
Aug 3, 2026
Start date
Jul 17, 2026
Primary completion
Mar 2028 (estimated)
Completion
Mar 2028 (estimated)
Last update
Aug 3, 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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