RECRUITING

Biopsychosocial Contributors to Irritability in Individuals With Shoulder 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

Irritability was defined by Geoffrey Maitland as the vigor of activity to provoke symptoms, the severity of symptoms, and time for symptoms to subside. Irritability is deeply embedded in the physical therapy clinical decision-making process. However, the mechanisms contributing to irritability are unknown. Therefore, the purpose of this study is to characterize pain sensitivity and pain-related psychological factors by irritability level in individuals with shoulder pain.

Official Title

Biopsychosocial Contributors to Irritability in Individuals With Shoulder Pain

Quick Facts

Study Start:2024-05-24
Study Completion:2026-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06429371

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 to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * shoulder pain symptom intensity rated as 3/10 or higher in the past 24 hours
  2. * attending physical therapy for shoulder pain
  1. * non-English speaking
  2. * systemic medical conditions that affect sensation, such as uncontrolled diabetes
  3. * history of shoulder surgery or fracture within the past 6 months
  4. * history of a chronic pain condition, such as fibromyalgia
  5. * blood clotting disorder, such as hemophilia
  6. * contraindication to the application of ice (blood pressure \> 140/90 mmHg, cold urticaria, cryoglobulinemia, paroxysmal cold hemoglobinuria, circulatory compromise)
  7. * currently pregnant

Contacts and Locations

Study Contact

Abigail W Anderson
CONTACT
4078231026
Abigail.Wilson@ucf.edu

Principal Investigator

Abigail Anderson
PRINCIPAL_INVESTIGATOR
University of Central Florida

Study Locations (Sites)

University of Central Florida
Orlando, Florida, 32765
United States

Collaborators and Investigators

Sponsor: University of Central Florida

  • Abigail Anderson, PRINCIPAL_INVESTIGATOR, University of Central Florida

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 Date2024-05-24
Study Completion Date2026-12-01

Study Record Updates

Study Start Date2024-05-24
Study Completion Date2026-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Shoulder Pain