NOT_YET_RECRUITING

Effects of a Mobile App-Based Mindfulness Intervention in Persons with Spinal Cord Injury and Chronic Pain

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Conditions

Spinal Cord Injuries

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to evaluate the efficacy of a 6-week app-guided MM intervention compared to a 6-week app-guided health education AC condition on pain intensity, pain interference, depression, and anxiety.

Official Title

Effects of a Mobile App-Based Mindfulness Intervention in Persons with Spinal Cord Injury and Chronic Pain: a Randomized Controlled Trial

Quick Facts

Study Start:2026-01-01
Study Completion:2029-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:NOT_YET_RECRUITING

Study ID

NCT06891989

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Traumatic SCI of at least 6 months duration
  2. * Chronic pain \[defined as pain lasting at least 3 months with a pain intensity rating of 4 or higher on a 10-point visual analog scale\]
  3. * Understand spoken and written English sufficiently to provide informed consent, participate in the intervention and complete study surveys
  1. * Lack of daily internet access
  2. * inability to demonstrate comprehension of informed consent by correctly answering 4 out of 5 questions about the study
  3. * Significant visual/hearing impairment that does not allow use of the MM app's audiovisual presentations
  4. * Use of any meditation more than once a week in the last 3 months
  5. * Inability to provide or obtain an email address for registration to the AC intervention and/or communication with study staff
  6. * inability to provide a phone number for communication with study staff

Contacts and Locations

Study Contact

Radha Korupolu, MD
CONTACT
713-797-5233
Radha.Korupolu@uth.tmc.edu
Shrasti Lohiya
CONTACT
713-797-7132
Shrasti.Lohiya@uth.tmc.edu

Principal Investigator

Radha Korupolu, MD
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Radha Korupolu, MD, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2026-01-01
Study Completion Date2029-12-30

Study Record Updates

Study Start Date2026-01-01
Study Completion Date2029-12-30

Terms related to this study

Additional Relevant MeSH Terms

  • Spinal Cord Injuries