True NTH Sexual Recovery Intervention for Prostate Cancer Survivors and Their Partners
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Prostate Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 6/21/2018 |
| Start Date: | March 2016 |
| End Date: | May 2019 |
There is increasing evidence that sexual activity is associated with greater resilience and
higher well-being in older adults. Even at a time of stress, and even during a late stage of
illness, men and their partners turn to sexual intimacy to increase a sense of connection,
comfort and support. The Sexual Recovery intervention seeks to address an unmet need of
prostate cancer survivors and their partners who are at risk for poor mental health and
decreased quality of life as a result of sexual dysfunction.
By using technology, the intervention will be widely accessible to survivors, the majority of
whom do not currently have any access to sexual health expertise. The content and format of
the intervention seeks to empower prostate cancer survivors and partners with knowledge and
strategies to improve their sexual function, sexual confidence and their sexual relationship.
The intervention begins prior to and continues following their definitive treatment. This
may, in turn, improve mental health and quality of life.
In a broader sense, this intervention will be transferable. With appropriate modifications,
it can become an accessible sexual health intervention for populations dealing with other
cancers and chronic illnesses.
higher well-being in older adults. Even at a time of stress, and even during a late stage of
illness, men and their partners turn to sexual intimacy to increase a sense of connection,
comfort and support. The Sexual Recovery intervention seeks to address an unmet need of
prostate cancer survivors and their partners who are at risk for poor mental health and
decreased quality of life as a result of sexual dysfunction.
By using technology, the intervention will be widely accessible to survivors, the majority of
whom do not currently have any access to sexual health expertise. The content and format of
the intervention seeks to empower prostate cancer survivors and partners with knowledge and
strategies to improve their sexual function, sexual confidence and their sexual relationship.
The intervention begins prior to and continues following their definitive treatment. This
may, in turn, improve mental health and quality of life.
In a broader sense, this intervention will be transferable. With appropriate modifications,
it can become an accessible sexual health intervention for populations dealing with other
cancers and chronic illnesses.
This proposal is innovative in a number of ways:
- The intervention is based on a full understanding of the complex nature of sexuality
with its bio- (functional), psycho- (confidence), and social (relationship components).
It incorporates modules that address each of these factors and their inter-dependencies.
- The intervention is sensitive to critical points in sexual recovery and to patient and
partner preferences in the context of therapies for prostate cancer. The intervention
acknowledges that there are certain time points at which concerns typically arise (e.g.,
when preparing for definitive treatment). The effectiveness of the intervention is
increased by the use of tailoring linked to patient reported outcomes (e.g., decreased
erectile function, increases in depression indices) and to patient/partner preferences.
- The intervention includes partners as equal stakeholders in the sexual recovery and
legitimizes their needs for sexual fulfillment and support
- The intervention demonstrates a sensitivity to sexual orientation and cultural diversity
- The intervention is scalable and available at limited or no cost to prostate cancer
survivors and their partners regardless of geographical location or system of care.
- The intervention is based on a full understanding of the complex nature of sexuality
with its bio- (functional), psycho- (confidence), and social (relationship components).
It incorporates modules that address each of these factors and their inter-dependencies.
- The intervention is sensitive to critical points in sexual recovery and to patient and
partner preferences in the context of therapies for prostate cancer. The intervention
acknowledges that there are certain time points at which concerns typically arise (e.g.,
when preparing for definitive treatment). The effectiveness of the intervention is
increased by the use of tailoring linked to patient reported outcomes (e.g., decreased
erectile function, increases in depression indices) and to patient/partner preferences.
- The intervention includes partners as equal stakeholders in the sexual recovery and
legitimizes their needs for sexual fulfillment and support
- The intervention demonstrates a sensitivity to sexual orientation and cultural diversity
- The intervention is scalable and available at limited or no cost to prostate cancer
survivors and their partners regardless of geographical location or system of care.
Inclusion Criteria:
- Patients diagnosed with localized prostate cancer who are about to receive definitive
treatment with either radiation with or without ADT (androgen deprivation therapy) or
prostatectomy AND who also have a spouse or been in a committed relationship with
their partner for at least 6 months who is willing to participate in the study. Both
parties are required to sign an informed consent, able to speak or read English, have
reliable internet access,have their own e-mail address, or be willing to sign up for a
new one, and must be 18 years of age or older. The participants must be consented at
least two weeks prior to the start of treatment, so that participants will have enough
time to complete a baseline survey and access the first module of the intervention.
Exclusion Criteria:
- Anyone unable to speak or read English, unwilling to sign an informed consent, under
the age of 18, or people without internet access will be excluded from the study.
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