Addressing Health Literacy With a Tailored Survivorship Care Plan

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorEmory University

About this trial

This clinical trial compares the impact of a tailored survivorship care plan (SCP) to a standard SCP on the understanding of and access to survivorship care in black or African American patients with prostate cancer that has not spread to other parts of the body (localized) or that has spread from where it first started (primary site) to a limited number of places in the body (oligometastatic). SCPs summarize treatment history and recommendations for monitoring and maintaining health, and may also include potential long term effects of treatments received. The intention of a SCP is to help patients participate in their own health care. However, many patients have below basic levels of health literacy, meaning, they have a lower ability to obtain, communicate, process and understand basic health information and services to make health decisions. In fact, poor health literacy has been linked with worse quality of life in prostate cancer survivors. A tailored SCP includes the addition of an educational supplement based on lower reading and writing skills (low literacy) and may address health literacy barriers to understanding of treatment options and side effects. A standard SCP uses a template based on the American Society of Clinical Oncology (ASCO) guidelines for prostate cancer. A tailored SCP with low literacy educational supplements may be more effective compared to a standard SCP in improving understanding and access to survivorship care in black or African American patients with localized or oligometastatic prostate cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Black and African American men who are disease-free after completing primary surgery and/or radiation treatment for localized or oligometastatic prostate cancer between 1 to 4 years prior to enrollment. (Race/ethnicity per medical records and self report)

Patients who are still receiving adjuvant androgen deprivation therapy following primary radiation with non-palliative intent may be included

Disqualifiers

Dementia or cognitive impairment per provider clinical assessment

Unable to give informed consent in the judgement of the patient's oncology provider

Recurrent prostate cancer after primary treatment

Less than 18 years of age at the time of informed consent

Trial design

Design model

Parallel

Treatments tested in this trial

  • Educational Intervention

    Other intervention

    Receive a low literacy educational supplement

  • Interview

    Other intervention

    Undergo a structured interview

  • Questionnaire Administration

    Other intervention

    Ancillary studies

  • Supportive Care

    Other intervention

    Receive standard SCP

  • Supportive Care

    Other intervention

    Receive a tailored SCP

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: Group I (standard SCP, tailored SCP)Experimental treatment 4 interventions
Group B: Group II (standard SCP)Active comparator 3 interventions

Trial outcomes

Primary outcomes

1

Comprehension of survivorship care recommendations and prostate specific antigen surveillance

Comprehension will be scored as dichotomous variables, correct or incorrect. The proportion of patients who correctly understand after the standard survivorship care plan (SCP) compared to the proportion who correctly understand after the standard SCP + tailoring + educational support will be analyzed using a two-tailed Z-score test for equality of two proportions at a significance level of P \< 0.05.

Time frame
At baseline and up to 3 month phone call
2

Comprehension of treatment side effects and late effects

Comprehension will be scored as dichotomous variables, correct or incorrect. The proportion of patients who correctly understand after the standard SCP compared to the proportion who correctly understand after the standard SCP + tailoring + educational support will be analyzed using a two-tailed Z-score test for equality of two proportions at a significance level of P \< 0.05.

Time frame
At baseline and up to 3 month phone call

Secondary outcomes

1

Access to survivorship care for late and long-term side effects

Will be assessed using the Patients Access Score (PAS). Descriptive statistics will be used to characterize patient access to survivorship care. The difference in mean PAS will be compared between the two arms using a 2 sample t-test. Results will be compared to previous studies, published work, and other historical cohorts. The concordance of urologists' assessment of patients' outcomes with outcomes obtained from patients will be analyzed as the percent of concordant responses, and with unweighted and weighted kappa coefficients. Linear regression models will be used to identify predictors of access to survivorship care. Parsimonious models will be favored due to the relatively small sample size.

Time frame
At baseline and up to 3 month phone call
2

Decision regret

Descriptive statistics will be used to characterize decision regret. Results will be compared to previous studies, published work, and other historical cohorts. The concordance of urologists' assessment of patients' outcomes with outcomes obtained from patients will be analyzed as the percent of concordant responses, and with unweighted and weighted kappa coefficients. Parsimonious models will be favored due to the relatively small sample size.

Time frame
At baseline and up to 3 month phone call
3

Change in decisional conflict

The two-sample t-test will be used to evaluate the change in the average decisional conflict score between patients in the control arm (standard SCP) and patients in the intervention arm (standard SCP + tailoring + educational supplement).

Time frame
At baseline and up to 3 month phone call
4

Preparedness for survivorship

Descriptive statistics will be used to characterize preparedness for survivorship. Results will be compared to previous studies, published work, and other historical cohorts. The concordance of urologists' assessment of patients' outcomes with outcomes obtained from patients will be analyzed as the percent of concordant responses, and with unweighted and weighted kappa coefficients. Parsimonious models will be favored due to the relatively small sample size.

Time frame
At baseline and up to 3 month phone call

Other outcomes

Sponsors and contacts

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Emory University

Lead sponsor

National Cancer Institute (NCI)

Collaborator

United States Department of Defense

Collaborator