RECRUITING

Our Whole Lives Gemini: Virtual Integrative Medical Group Visits for Managing Chronic Pain

Conditions

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 goal of this research study is to test the efficacy of a non-prescription medicine, web-based platform solution for patients with chronic pain, to improve pain self-management and related outcomes. The main question investigators aim to answer is; would the use of this web-based intervention plus an online group visit compared to control result in better pain-related outcomes and improved pain impact?

Official Title

Phase II: GEMINI: Virtual Integrative Medical Group Visits for Managing Chronic Pain

Quick Facts

Study Start:2024-08-01
Study Completion:2025-11-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06515925

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. * English-speaking adults
  2. * Over the age of 18
  3. * Experiencing chronic musculoskeletal pain. (Pain may have more than one source; Pain must be non-malignant; Participant must have an average pain intensity of ≥ 4 (1 out of 10) in the past 7 days; Participant must meet the chronic criteria of a pain problem that has persisted at least 3 months, and has resulted in pain on at least half the days in the past 6 months)
  1. * Inability to understand English at a level necessary for informed consent and understanding participation instructions, and participating in the group;
  2. * Serious underlying systemic or co-morbid conditions or life event that precludes physical or cognitive ability to participate in the study.
  3. * Severe depression
  4. * Current mania or psychosis;
  5. * Active heroin or cocaine use in the past 3 months
  6. * Heavy alcohol use
  7. * Known or planned pregnancy

Contacts and Locations

Study Contact

Tori Blot
CONTACT
8572858961
toblot@challiance.org
Alexandra Comeau
CONTACT
617-806-8735
acomeau@challiance.org

Principal Investigator

Zev Schuman-Olivier, MD
STUDY_DIRECTOR
Cambridge Health Alliance
Paula Gardiner, MD, MPH
PRINCIPAL_INVESTIGATOR
Cambridge Health Alliance
Niina Haas, PHD
PRINCIPAL_INVESTIGATOR
BrightOutcome

Study Locations (Sites)

Cambridge Health Alliance Center for Mindfulness and Compassion
Malden, Massachusetts, 02458
United States

Collaborators and Investigators

Sponsor: Cambridge Health Alliance

  • Zev Schuman-Olivier, MD, STUDY_DIRECTOR, Cambridge Health Alliance
  • Paula Gardiner, MD, MPH, PRINCIPAL_INVESTIGATOR, Cambridge Health Alliance
  • Niina Haas, PHD, PRINCIPAL_INVESTIGATOR, BrightOutcome

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 Date2024-08-01
Study Completion Date2025-11-30

Study Record Updates

Study Start Date2024-08-01
Study Completion Date2025-11-30

Terms related to this study

Additional Relevant MeSH Terms

  • Chronic Pain