SuspendedNot Applicable

MBCT-T for Preoperative Pain Catastrophizing and Pain Outcomes After Spine Surgery

Stopped: Temporarily suspended.

United States25 participantsStarted 2020-01-09

Plain-language summary

This is a two phase study. In phase 1, a focus group (N=5) will be conducted to adapt MBCT-T for use in the study population. In phase 2, a single-arm trial will be conducted examining four, weekly sessions of preoperative MBCT-T in subjects with high pain catastrophizing scheduled for spine surgery (N=20). Subjects will then be followed for two weeks postoperatively.

Who can participate

Age range18 Years – 75 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: * Scheduled for one or two level lumbar spine surgery requiring an inpatient stay as well as patients having ambulatory 1 or 2 level lumbar spine surgeries * PCS score ≥ 20 * Able to provide voluntary informed consent * Telephone access * Internet access Exclusion Criteria: * Non-English speaking * Cognitively impaired, by history * Bipolar disorder * Borderline personality disorder * Active post-traumatic stress disorder * Schizoaffective disorder or any other disorder characterized by delusions or hallucinations * History of self-harm or suicidality in past three months

What they're measuring

Percentage of Participants who Attend More than Half of Scheduled Sessions

Timeframe: Up to Week 8 (End of Intervention)

Client Satisfaction Questionnaire (CSQ-8) Score

Timeframe: Week 8 (End of Intervention)

Trial details

NCT IDNCT05888025

SponsorNYU Langone Health

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-06

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