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

Completed
Conditions
Sexual Dysfunction
Interventions
Behavioral: Patient's Perspective
Registration Number
NCT05837117
Lead Sponsor
M.D. Anderson Cancer Center
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.

Detailed 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 & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
104
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
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Exclusion Criteria

Not provided

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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Patient's PerspectivePatient's PerspectiveParticipants 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.
Primary Outcome Measures
NameTimeMethod
Quality of Life Questionnairesthrough study completion an average of year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

M D Anderson Cancer Center

🇺🇸

Houston, Texas, United States

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