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CompletedNCT06265376Updated Aug 23, 2024

Do Patient Educational Videos Improve Pain and Recovery After Laparoscopic Hysterectomy?

An interventional study of Educational Video in Pain, Postoperative, sponsored by Benaroya Research Institute. Completed at 1 site in United States. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-23.

Sponsored by Benaroya Research Institute · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Mar 2023, registered Jan 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study summary

The use of multi-model patient education has been used in a variety of medical specialties to educate patients on expectations for various medical procedures and improve patients' understanding of their own health care. However, it is unknown what type of audio and/or visual materials work best in a given clinical setting. By surveying overall pain/post-operative recovery satisfaction we can measure how well our video intervention educates and reinforces post-operative management at home when compared to the current method of education that patients receive at the pre-operative visit prior to laparoscopic hysterectomy at this institution.

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Conditions studied

  • Pain, Postoperative

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03

In context

Pain, Postoperative

5,089 studies on the registry are indexed under Pain, Postoperative; 1,137 are open to participants now.

This study's enrollment of 94 is above the median of 75 across 4,341 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Benaroya Research Institute is the lead sponsor of 41 studies on the registry; 6 are open to participants now.

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
Yes

Inclusion criteria

  • 18y/o or older
  • planned for a laparoscopic hysterectomy for benign indications

Exclusion criteria

Exclusion Criteria:

  • inability to consent
  • language other than English
  • conversion to laparotomy, vNOTES (a type of laparoscopic assisted vaginal hysteroectomy)
  • vaginal hysterectomy
  • chronic opioid use prior to surgery
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Study design

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

Study arms

  • Experimental
    Educational Video Intervention

    Participants have been randomly selected into this arm to receive intervention via the educational video in addition to regular treatment and recovery options.

    Behavioral: Educational Video

  • No intervention
    No Intervention

    Participants have been randomly selected into this arm to not receive intervention and continue with regular treatment and recovery options.

Interventions

  • BehavioralEducational Video

    A recorded educational video will be presented to the patient prior to meeting with the provider at the presurgical meeting

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What researchers measure

Primary outcomes

  1. Overall satisfaction score (5 point Likert scale) with post operative pain control after laparoscopic hysterectomy

    To determine if video education on post-operative pain management and expectations can improve patients' overall satisfaction with post operative pain control after laparoscopic hysterectomy

    Time frame: Within 10 days post surgery

Secondary outcomes

  1. Pain score at the time of survey completion (0=no pain 10=worst pain

    To determine if video education on post-operative pain management and expectations improves patient post operative pain scores at the time of post-op phone call

    Time frame: Within 10 days post surgery

  2. Average pain score for the first 7 days as perceived by the patients (likert scale)

    To determine if video education on post-operative pain management and expectations improves patient perceived post operative pain control throughout the first 7 day post-op

    Time frame: Within 10 days post surgery

  3. Number of post-op phone calls received

    To determine if video education on post-operative pain management and expectations decreases the number of post- operative phone calls received by providers during the first week post-op

    Time frame: Within 10 days post surgery

  4. Number of post-op emergency room visits

    To determine if video education on post-operative pain management and expectations decreases the number of post- operative emergency room visits by patients during the first week post-op

    Time frame: Within 10 days post surgery

  5. Number of readmissions

    To determine if video education on post-operative pain management and expectations decreases the number of postoperative readmissions by patients during the first week post-op

    Time frame: Within 10 days post surgery

  6. Number of patients with steri-strips still in place

    To determine if video education on post-operative pain management and expectations decreases the number of patients who have not removed their steri-strips by day 7

    Time frame: Within 10 days post surgery

  7. Number opioids taken since surgery

    To determine if video education on post-operative pain management and expectations decreased the number of narcotics used post-operatively

    Time frame: Within 10 days post surgery

  8. Overall satisfaction with pre-operative education regarding surgery (5 point Likert scale)

    To determine if video education on post-operative pain management and expectations improves overall satisfaction with pre-operative education regarding surgery

    Time frame: Within 10 days post surgery

  9. ding surgery (5 point likert scale) Overall satisfaction with educations regarding what to expect post-operatively (5 point Likert scale)

    To determine if video education on post-operative pain management and expectations improves overall satisfaction with educations regarding what to expect post-operatively

    Time frame: Within 10 days post surgery

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Study locations

1 site
  • Virginia Mason Medical Center
    Seattle, Washington 98101, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 23, 2024, 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
NCT06265376
Lead sponsor
Benaroya Research Institute
Responsible party
Megan Loring (MD, Gynecologist, Benaroya Research Institute) — Principal investigator
First posted
Feb 20, 2024
Start date
Mar 13, 2023
Primary completion
Apr 28, 2024
Completion
Apr 28, 2024
Last update
Aug 23, 2024

Study contacts

Megan Loring, MD
principal investigator · Virginia Mason Medical Center

Oversight

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

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This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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