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

NCT05837117 | Completed

• 2 other identifiers: 2022-0495NCI-2022-10774
• Study Type: observational
• Target: 104
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Sexual Dysfunction

Outcome Measures

Primary Outcomes (1)

• Quality of Life Questionnaires

  through study completion an average of year

Study Arms (1)

Patient's Perspective

Participants will complete a questionnaire about sexual wellbeing, sexual dysfunction, and communication with your provider on this topic. Participants may choose to complete the questionnaire electronically (via email link), in-person, or over the phone, whichever you prefer. Your demographic information (such as age, gender, ethnicity, marital status, and cancer diagnosis) will be collected from your medical record. Some of this information may also be asked of you during the questionnaire.

Behavioral: Patient's Perspective

Interventions

Patient's Perspective BEHAVIORAL

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

Patient's Perspective

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

M D Anderson Cancer Center

You may qualify if:

• 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

You may not qualify if:

• New patients (consults)
• Patient who have declined to participate, or who are unable to consent

Sponsors & Collaborators

• M.D. Anderson Cancer Center: lead

Study Sites (1)

M D Anderson Cancer Center

Houston, Texas, 77030, United States

Location

Related Links

• M D Anderson Cancer Center

MeSH Terms

Conditions

Sexual Dysfunction, Physiological

Condition Hierarchy (Ancestors)

Genital Diseases; Urogenital Diseases

Study Officials

• Patricia Bramati, MD

  M.D. Anderson Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 19, 2023
• First Posted: May 1, 2023
• Study Start: December 15, 2022
• Primary Completion: December 13, 2024
• Study Completion: December 13, 2024
• Last Updated: December 19, 2024

Record last verified: 2024-12

Locations

US (1)