MedTrace Logo

A Behavioral Intervention for Pain Catastrophizing in Primary Dysmenorrhea

NCT02640079 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2018-04-13

No results posted yet for this study

Summary

The purpose of this study is to test the feasibility and efficacy of a brief group therapy treatment program focused on reducing pain catastrophizing in adolescents and young adults (ages 16-25) with menstrual pain.

Conditions

  • Pain Catastrophizing
  • Primary Dysmenorrhea

Interventions

BEHAVIORAL

Cognitive behavioral therapy

Sponsors & Collaborators

Principal Investigators

  • Laura A Payne, PhD · University of California, Los Angeles

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Max Age
25 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-11-30
Completion
2017-11-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02640079 on ClinicalTrials.gov