By InvitationNot Applicable

Perioperative Sleep Quality and Postoperative Pain Outcomes

United States166 participantsStarted 2025-02-03

Plain-language summary

This is a prospective, observational cohort study that will examine how sleep quality impacts postoperative pain and opioid consumption for pediatric patients. The investigators will administer a questionnaire preoperatively to determine which patients have poor or good sleep quality. They will then compare postoperative pain and opioid use between groups for two weeks following surgery. For a secondary aim, investigators will use electronic medication vials (eCAP) to monitor participants' medication use at home and compare to self-reporting.

Who can participate

Age range10 Years – 18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * able to read, understand, and speak English * are undergoing posterior spinal fusion surgery * have availability of a mobile device/computer to receive text messages Exclusion Criteria: * \< 10 or \> 18 years of age * have a history of sleep-disordered breathing including sleep apnea * have a history of chronic pain or current opioid use * have a history of developmental delay that would preclude study participation

What they're measuring

Pittsburgh Sleep Quality Index

Timeframe: Baseline

Difference in opioid consumption between self-report and eCap

Timeframe: Days 1-14 post-op

Trial details

NCT IDNCT06054802

SponsorGrant Heydinger

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-12

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