--- title: Meditation Effects on Discomfort, Pain InTerference, and AnxieTy After urEteroscopy nct_id: NCT06783946 overall_status: ENROLLING_BY_INVITATION phase: NA sponsor: "Children's Hospital of Philadelphia" study_type: INTERVENTIONAL primary_condition: Kidney Stone countries: United States canonical_url: "https://parkinsonspathways.com/agent/trials/NCT06783946.md" clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT06783946" ct_last_update_post_date: 2025-12-04 last_seen_at: "2026-05-12T07:01:14.185Z" source: ClinicalTrials.gov (mirrored, no enrichment) --- # Meditation Effects on Discomfort, Pain InTerference, and AnxieTy After urEteroscopy **Official Title:** The Effect of Meditation on Anxiety and Pain of Patients Undergoing Ureteroscopy for Kidney Stones: A Pilot Randomized Study **NCT ID:** [NCT06783946](https://clinicaltrials.gov/study/NCT06783946) ## Key Facts - **Status:** ENROLLING_BY_INVITATION - **Phase:** NA - **Study Type:** INTERVENTIONAL - **Target Enrollment:** 50 - **Lead Sponsor:** Children's Hospital of Philadelphia - **Collaborators:** University of Pennsylvania - **Conditions:** Kidney Stone, Pain, Postoperative, Anxiety Postoperative - **Start Date:** 2024-12-02 - **Completion Date:** 2026-07-31 - **CT.gov Last Update:** 2025-12-04 ## Brief Summary The goal of this pilot clinical trial is to learn whether meditation can help improve recovery in children and adults having surgery for kidney stones. The main questions it aims to answer are: * Does meditation around the time of surgery improve pain and anxiety in patients undergoing kidney stone surgery (ureteroscopy)? * Is a meditation program around the time of surgery feasible for patients having kidney stone surgery (ureteroscopy)? Participants will be randomly assigned to the meditation group and the control group to understand how meditation affects recovery after surgery. Participants will be asked to: * Complete a health history form * Complete questionnaires about pain and mood before surgery and certain days after surgery * Those in the meditation group will learn and practice a daily 20-minute meditation for 2-4 weeks before surgery and 2 weeks after surgery * Those in the meditation group will be asked to provide feedback of the meditation program after completing the last questionnaire ## Detailed Description Context: Pain is common after surgery to remove urinary stones, and current options for post-operative pain management are limited. Pre-operative anxiety is a well-known clinical entity that is associated with a higher risk of post-operative pain. Meditation is an ancient discipline that has been used for a wide range of presumed benefits including improving pain and anxiety. Meditation has been studied in a variety of clinical settings, but its effects have not been assessed among patients having ureteroscopy to remove kidney and/or ureteral stones. Objectives: To determine the effect of a peri-operative meditation intervention on physical and emotional health in adolescent and adult patients undergoing elective unilateral ureteroscopy for unilateral renal or ureteral stones. To determine the feasibility of implementing a perioperative meditation intervention in patients undergoing elective unilateral ureteroscopy for ureteral or renal stones Study Design: Pilot randomized controlled trial Setting/Participants: This study will recruit 50 patients aged 12 years or older at the Children's Hospital of Philadelphia and University of Pennsylvania, who will be undergoing elective unilateral ureteroscopy for unilateral renal or ureteral stones with or without stent placement. Participants will be randomized to the meditation intervention or usual care treatment arms. Intervention: Participants will be randomized to the intervention (meditation) or control groups. Participants will learn and practice a daily 20-minute meditation for 2-4 weeks before scheduled surgery (whichever is the maximum length of time from enrollment) to 2 weeks post-operatively using the provided audio guide. The Patient-Reported Outcomes Measurement Information System (PROMIS) instruments in the domains of Pain Intensity, Pain Interference, Anxiety, and Depression will be utilized. Patients will complete the questionnaire at the time of enrollment, and at post-operative days 3, 14, and 30. General information, health history, and kidney stone related events will be assessed from the medical record. ## Eligibility - **Minimum age:** 12 Years - **Sex:** ALL - **Healthy Volunteers:** Yes ``` Inclusion Criteria: 1. Subjects age 12 years and older 2. Diagnosis of unilateral or bilateral ureteral or renal stones 3. Scheduled to undergo elective unilateral ureteroscopy for renal or ureteral stones in 2 or more weeks from initial clinic visit 4. Parental/guardian permission (informed consent) and if appropriate, child assent. Exclusion Criteria: 1. Participants \<12 years of age 2. Subjects undergoing any other type of stone procedure (i.e. bilateral ureteroscopy, percutaneous nephrolithotomy, ESWL, staged ureteroscopy) 3. Patients who are pre-stented at the initial clinic visit 4. Non-English speaking participants 5. Participants without functional e-mail address or phone 6. Participants unable to use a computer/tablet independently 7. Participants who will be undergoing ureteroscopy in less than 2 weeks from initial clinic visit 8. Patients who are non-verbal or with cognitive delay that may impair ability to learn and adhere to intervention 9. Patients with neurologic comorbidities that may alter sensation (eg. spinal cord injuries) 10. Parents/guardians or subjects who, in the opinion of the investigator, may be non-compliant with study schedules or procedures ``` ## Arms - **Meditation** (EXPERIMENTAL) — In the intervention group, a meditation intervention will be implemented pre- and post-operatively. The meditation technique will be comprised of breathing techniques, full body relaxation, color meditation, visualization, and positive affirmations. A physician researcher trained in teaching meditation will conduct virtual meditation sessions with patients enrolled in the study. Participants will practice a daily 20-minute meditation for 2-4 weeks before scheduled surgery (whichever is the maximum length of time from enrollment) to 2 weeks post-operatively using the provided audio guided meditation recordings. Participants will also log adherence to meditation via daily questionnaires. They will receive standard pre-operative counseling and post-operative medications at the discretion of their urologist. - **Usual Care** (NO_INTERVENTION) — Those in the control or usual care arm will complete the same questionnaires at baseline and at post-operative days 3, 14, and 30. They will receive standard pre-operative counseling and post-operative medications at the discretion of their urologist. ## Interventions - **Meditation** (BEHAVIORAL) — The meditation technique will be comprised of breathing techniques, full body relaxation, color meditation, visualization, and positive affirmations. A physician researcher trained in teaching meditation will conduct virtual meditation sessions with patients enrolled in the study. Participants will practice a daily 20-minute meditation for 2-4 weeks before scheduled surgery (whichever is the maximum length of time from enrollment) to 2 weeks post-operatively using the provided audio guided meditation recordings. Participants will also log completion of daily meditation practice electronically. ## Primary Outcomes - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 3 (Pain Intensity)** _(time frame: Pre-operative baseline to post-operative day 3)_ — The primary outcome is the change in PROMIS T-scores from pre-operatively to post-operative day 3 in the domains of pain intensity, pain interference, anxiety, and depression. Four PROMIS questionnaires will be utilized, one for each domain. Questionnaires will be administered electronically with computerized adaptive testing (CAT). With CAT participants' responses guide the system's choice of subsequent items from the question bank; therefore, there is not a set number of questions per respondent. Each questionnaire will typically consist of 4-12 items and can be completed under 1 minute. Each questionnaire results in a standardized T-Score, in which 50 is the mean score for a general reference population, and 10 is the standard deviation. A higher PROMIS T-score represents more of the concept being measures (e.g. worse anxiety or pain intensity). Questionnaires will be administered at baseline and post-operative days 3, 14, 30 with separate T-scores for each time point and domain. - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 3 (Pain Interference)** _(time frame: Pre-operative baseline to post-operative day 3)_ — The primary outcome is the change in PROMIS T-scores from pre-operatively to post-operative day 3 in the domains of pain intensity, pain interference, anxiety, and depression. Four PROMIS questionnaires will be utilized, one for each domain. Questionnaires will be administered electronically with computerized adaptive testing (CAT). With CAT participants' responses guide the system's choice of subsequent items from the question bank; therefore, there is not a set number of questions per respondent. Each questionnaire will typically consist of 4-12 items and can be completed under 1 minute. Each questionnaire results in a standardized T-Score, in which 50 is the mean score for a general reference population, and 10 is the standard deviation. A higher PROMIS T-score represents more of the concept being measures (e.g. worse anxiety or pain intensity). Questionnaires will be administered at baseline and post-operative days 3, 14, 30 with separate T-scores for each time point and domain. - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 3 (Anxiety)** _(time frame: Pre-operative baseline to post-operative day 3)_ — The primary outcome is the change in PROMIS T-scores from pre-operatively to post-operative day 3 in the domains of pain intensity, pain interference, anxiety, and depression. Four PROMIS questionnaires will be utilized, one for each domain. Questionnaires will be administered electronically with computerized adaptive testing (CAT). With CAT participants' responses guide the system's choice of subsequent items from the question bank; therefore, there is not a set number of questions per respondent. Each questionnaire will typically consist of 4-12 items and can be completed under 1 minute. Each questionnaire results in a standardized T-Score, in which 50 is the mean score for a general reference population, and 10 is the standard deviation. A higher PROMIS T-score represents more of the concept being measures (e.g. worse anxiety or pain intensity). Questionnaires will be administered at baseline and post-operative days 3, 14, 30 with separate T-scores for each time point and domain. - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 3 (Depression)** _(time frame: Pre-operative baseline to post-operative day 3)_ — The primary outcome is the change in PROMIS T-scores from pre-operatively to post-operative day 3 in the domains of pain intensity, pain interference, anxiety, and depression. Four PROMIS questionnaires will be utilized, one for each domain. Questionnaires will be administered electronically with computerized adaptive testing (CAT). With CAT participants' responses guide the system's choice of subsequent items from the question bank; therefore, there is not a set number of questions per respondent. Each questionnaire will typically consist of 4-12 items and can be completed under 1 minute. Each questionnaire results in a standardized T-Score, in which 50 is the mean score for a general reference population, and 10 is the standard deviation. A higher PROMIS T-score represents more of the concept being measures (e.g. worse anxiety or pain intensity). Questionnaires will be administered at baseline and post-operative days 3, 14, 30 with separate T-scores for each time point and domain. ## Secondary Outcomes - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 30 (Pain Intensity)** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 30 (Pain Interference)** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 30 (Anxiety)** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Change in PROMIS Scores from Pre-Operatively to Post-Operative Day 30 (Depression)** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Feasibility Outcome: Monthly Proportion of Enrolled to Eligible Participants** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Feasibility Outcome: Completion of Questionnaires** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Feasibility Outcome: Meditation Adherence** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Number of Participants Who Sought Unplanned Medical Attention** _(time frame: Pre-operative baseline to 1 month post-operatively)_ - **Medication usage** _(time frame: From surgery to post-operative day 30)_ ## Locations (2) - Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States - University of Pennsylvania, Philadelphia, Pennsylvania, United States ## Recent Field Changes (last 30 days) - `status.overallStatus` — added _(2026-05-12)_ - `status.primaryCompletionDate` — added _(2026-05-12)_ - `status.completionDate` — added _(2026-05-12)_ - `status.lastUpdatePostDate` — added _(2026-05-12)_ - `design.phases` — added _(2026-05-12)_ - `design.enrollmentCount` — added _(2026-05-12)_ - `eligibility.criteria` — added _(2026-05-12)_ - `eligibility.minAge` — added _(2026-05-12)_ - `eligibility.sex` — added _(2026-05-12)_ - `outcomes.primary` — added _(2026-05-12)_ - `outcomes.secondary` — added _(2026-05-12)_ - `armsInterventions.arms` — added _(2026-05-12)_ - `armsInterventions.interventions` — added _(2026-05-12)_ - `sponsor.lead` — added _(2026-05-12)_ - `sponsor.collaborators` — added _(2026-05-12)_ - `results.hasResults` — added _(2026-05-12)_ - `locations.children's hospital of philadelphia|philadelphia|pennsylvania|united states` — added _(2026-05-12)_ - `locations.university of pennsylvania|philadelphia|pennsylvania|united states` — added _(2026-05-12)_ --- *Canonical: https://parkinsonspathways.com/agent/trials/NCT06783946.md* *Source data (authoritative): https://clinicaltrials.gov/study/NCT06783946* *This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*