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NCT05837117 Clinical Trial

Sexual Dysfunction in Palliative Care Patients: An Assessment of Patient's Perspective

Sexual Dysfunction Clinical Trial

Official title:
Sexual Dysfunction in Palliative Care Patients: An Assessment of Patient's Perspective

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05837117
Other study ID # 2022-0495
Secondary ID NCI-2022-10774
Status Active, not recruiting
Phase
First received
Last updated
Start date December 15, 2022
Est. completion date June 1, 2025

Study information
Verified date February 2024
Source M.D. Anderson Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To learn about the communications that Supportive Care patients receive about sexual well-being from their healthcare provider. Researchers also want to learn about your attitudes, beliefs, and feelings about sexual well-being.

Description:

Primary Objectives: 1. To determine the frequency of discussion about sexual dysfunction in palliative care patients. 2. To evaluate the impact of cancer diagnosis and treatment on patient's sexual life. Secondary Objectives: 1. To evaluate patient self-reported severity of sexual dysfunction 2. To evaluate the proportion of patients suffering distress from body image concerns 3. To identify patient self-reported barriers that prevent discussion about sexual dysfunction 4. To evaluate patient self-reported impact of sexual dysfunction on their wellbeing

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 150
Est. completion date June 1, 2025
Est. primary completion date June 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All patients who are evaluated as follow-ups in the Supportive Care clinic, and able to voluntarily consent to participate in the study - Patients must be able to understand, read, write, and speak English - Diagnosis of cancer - Patients who are 18 years of age or older Exclusion criteria: - New patients (consults) - Patient who have declined to participate, or who are unable to consent

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Patient's Perspective
Participants will complete a questionnaire about sexual wellbeing, sexual dysfunction, and communication with your provider on this topic. Participants/Researchers will learn about your attitudes, beliefs, and feelings about sexual well-being

Locations
Country Name City State
United States M D Anderson Cancer Center Houston Texas

Sponsors (1)
Lead Sponsor Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Quality of Life Questionnaires through study completion an average of year
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