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Short video before surgery boosts recovery and eases anxiety, study finds

NCT ID NCT07364968

Symptom relief Sponsor: University of California, Riverside Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a short instructional video watched before minimally invasive gynecologic surgery helps patients feel more prepared and recover better. About 57 women participated, with some watching the video and others not. Researchers measured anxiety, pain, medication use, and satisfaction to see if the video made a difference.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

57 people

The number who actually took part.

Started

Sep 2023

Finished

Apr 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

Up to 18 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Participants/Sample Size: Female patients who have been recommended for minimally invasive gynecologic surgery. A total of 52 patients will be enrolled in this study at UCR Women's Health Clinic. Statistical power: To detect an effect size of 0.5 with a power of 0.8, a sample size of 52 participants was required. Inclusion criteria: * Age 18 - 65 years old * Surgery with UCR Gynecology physician * Laparoscopic/robotic surgery * Same day discharge after surgery * Can read a survey in English * Female Exclusion Criteria: * Receiving postoperative chemotherapy in the 6-week postoperative period * Minors under the age of 18 * Postoperative overnight stay * Laparotomy (open surgery) * Pregnancy

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Gynecologic laparoscopic surgery Minimally invasive surgical procedures

Contacts and locations

Locations

  • University of Riverside, California

    Riverside, California, 92521, United States

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