Know Cancer

or
forgot password


N/A
N/A
N/A
Not Enrolling
Both
Prostate Cancer

Thank you

Trial Information


Inclusion Criteria:



- Men who have been treated for localized prostate cancer

- AND men must be 6-36 months post-prostatectomy or radiation (as primary treatment) of
prostate cancer

- Must have a heterosexual, co-cohabiting partner who is willing to participate

- Must speak and read English

- Must be able to use a computer and have internet access

Exclusion Criteria:

- Homosexual couples will not be included in this study

- Major self-reported psychiatric illness

- Couples who screen below 30 on the DAS (Dyadic Adjustment Scale)

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Outcome Measure:

Change in Sexual Function from Baseline to 13 weeks

Outcome Time Frame:

Pre-Intervention (Week 1); Post-Intervention (Week 7); 3 Months Post-Intervention (Week 13)

Safety Issue:

No

Principal Investigator

Deborah L McLeod, R.N., Ph.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

Capital District Health Authority & Dalhousie University

Authority:

Canada: Capital District Health Authority REB

Study ID:

CDHA-RS/2013-076

NCT ID:

NCT01716702

Start Date:

November 2012

Completion Date:

January 2014

Related Keywords:

  • Prostate Cancer
  • Prostate Cancer
  • Psychosocial Intervention
  • Sexual Rehabilitation
  • Online Intervention
  • Prostatic Neoplasms

Name

Location