Chronic Non-Malignant Pain in Cancer Patients at a Supportive Care Clinic

NCT ID: NCT03043378

Last Updated: 2023-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

201 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-07-31

Study Completion Date

2023-03-23

Brief Summary

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The goal of this research study is to learn how frequently cancer patients in the Supportive Care Center have chronic, non-malignant pain. Chronic, non-malignant pain is pain that is neither related to cancer nor its treatment and lasts beyond the normal tissue healing time of 3 months.

Detailed Description

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If participant is found to be eligible and agrees to take part in this study, participant will be asked to complete 3 questionnaires about participant's pain, pain level, and what drugs participant takes to treat participant's pain. Participant will also be asked a few questions about tobacco use. These questionnaires should take about 20 minutes to complete.

Researchers will also collect information from participant's medical record such as participant's date of birth, sex, race, marital status, economic background, and medical history.

Length of Study:

Participation on this study will be over after participant has completed the last questionnaire.

This is an investigational study.

Up to 200 participants will be enrolled in this study. All will take part at MD Anderson.

Conditions

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Malignant Neoplasms of Independent (Primary) Multiple Sites

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Chronic Non-Malignant Pain - Cancer Patients

Chronic non-malignant pain among cancer patients undergoing a consultation at the outpatient Supportive Care Clinic at MD Anderson Cancer Center.

Questionnaires

Intervention Type BEHAVIORAL

Participants complete three questionnaires at consultation visit.

Interventions

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Questionnaires

Participants complete three questionnaires at consultation visit.

Intervention Type BEHAVIORAL

Other Intervention Names

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Surveys

Eligibility Criteria

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Inclusion Criteria

1. Diagnosis of cancer with or without active disease
2. Consultation visit at an outpatient supportive care clinic
3. Age 18 or greater
4. Report of having pain within the last 3 months

Exclusion Criteria

1\) Memorial Delirium Assessment Scale \>13
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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David Hui, MD

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

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University of Texas MD Anderson Cancer Center

Houston, Texas, United States

Site Status

Countries

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United States

Related Links

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http://www.mdanderson.org

University of Texas MD Anderson Cancer Center Website

Other Identifiers

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NCI-2018-01268

Identifier Type: REGISTRY

Identifier Source: secondary_id

2016-0901

Identifier Type: -

Identifier Source: org_study_id

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