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NCT05346692 · ClinicalTrials.gov registry record · Early Phase 1

Digital Meditation for Postoperative Pain Control After Abdominal Surgery for Cancer

A Early Phase 1 study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid System Neoplasm, sponsored by Emory University.

Completed
Registry status
Early Phase 1
Development phase
73
Enrollment target
1
Study location

NCT05346692 is a Early Phase 1 study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid System Neoplasm that has completed, run by Emory University. The registered enrollment target is 73 participants, below the 1,140-participant average among 176 other Malignant Solid Neoplasm trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05346692, a Early Phase 1 study of Malignant Solid Neoplasm and Hematopoietic and Lymphoid System Neoplasm, has completed, sponsored by Emory University.

COMPLETED
Registry status
Early Phase 1
Development phase
73 participants
Enrollment target
1
Study location

Study Summary

This phase I trial tests a digital meditation for postoperative pain control after abdominal surgery for cancer. Mindfulness interventions such as guided meditation may improve pain control and decrease stress. Including a brief mindfulness intervention administered via test messages as part of postoperative care may improve pain severity, decrease opioid use, and improve patient responses to non-surgical treatments.

Interventions

  • OTHER Survey Administration
  • OTHER Interview
  • OTHER Text Message-Based Navigation Intervention

Study Locations (1)

Georgia

  • Emory University/Winship Cancer Institute - Atlanta

Trial Details

FieldValue
Enrollment Target 73 participants
Start Date 2022-03-28
Est. Completion 2023-07-12
Phase Early Phase 1

Sponsor

Emory University

1,208 total trials

What the Registry Record Tells You About NCT05346692

The ClinicalTrials.gov registry entry for NCT05346692 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 73 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,140-participant average among 176 other Malignant Solid Neoplasm trials with a reported enrollment target (94% lower). The listed sponsor is Emory University, which has 1,208 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Malignant Solid Neoplasm appearing as the primary indexed condition, and to 3 interventions - of which Survey Administration is the first listed.

NCT05346692 reports 1 study location spanning 1 distinct geographic area - top geographies include Georgia.

Frequently Asked Questions

What is clinical trial NCT05346692 about?

NCT05346692 is a clinical study titled "Digital Meditation for Postoperative Pain Control After Abdominal Surgery for Cancer". This phase I trial tests a digital meditation for postoperative pain control after abdominal surgery for cancer. Mindfulness interventions such as guided meditation may improve pain control and decrease stress. Including a brief mindfulness intervention administered via test messages as part of post...

What is the current status of trial NCT05346692?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 73 participants. The study started on 2022-03-28. Estimated completion is 2023-07-12.

What conditions does trial NCT05346692 study?

This clinical trial studies the following conditions: Malignant Solid Neoplasm, Hematopoietic and Lymphoid System Neoplasm.

What interventions are being tested in trial NCT05346692?

The interventions under investigation include: Survey Administration (OTHER), Interview (OTHER), Text Message-Based Navigation Intervention (OTHER).

Who is sponsoring clinical trial NCT05346692?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05346692 being conducted?

This trial has 1 study location across Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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