Clinical trial · Interventional
A Pilot Study of Prostate Cancer-specific Anxiety in Active Surveillance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Study has been terminated
Summary
Brief summary (as posted)
This study is a clinical trial to determine whether a 12-week group therapy intervention for patients undergoing Active Surveillance for Prostate Cancer can relieve disease-related anxiety and improve quality of life and delay elective treatment of prostate cancer. The goal of the study is to further our understanding of anxiety in men who have been diagnosed with prostate cancer and are undergoing Active Surveillance. Men who have elected Active Surveillance for their management of prostate cancer are eligible to participate in this study. After signing informed consent, all participants will complete two brief questionnaires (The Memorial Anxiety Scale for Prostate Cancer \[MAX-PC\] and the General Anxiety and Depression Scale 7 \[GAD-7\] to measure their anxiety levels. If the participant scores above a certain number, they will be asked to participate in the study. Patients will be randomly assigned to either a control group, who will receive no treatment, but continue to follow up with their urologist to manage their prostate cancer as usual, or the treatment group. The treatment group will receive 12 one-hour group therapy sessions that will take place once a week for 12 weeks with a licensed psychologist free of charge. They will be instructed to follow up with their urologist as previously determined for their prostate cancer management. Patients in both groups will be monitored for anxiety completing three questionnaires, the MAX-PC and GAD-7 which they previously completed, and the Functional Assessment of Cancer Therapy - Prostate (FACT-P) during the 4th and 12th weeks of therapy. If patients require further therapy beyond the group treatment sessions, the investigators may refer them to a psychologist or psychiatrist for further treatment.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Group therapy | Behavioral | — | UNRESOLVED |
| Surveys | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Enrolled in group therapy
- description
- Patients in the group therapy arm will be enrolled in group therapy and be issued surveys.
- interventionNames
- Behavioral: Group therapy
- Other: Surveys
- type
- PLACEBO_COMPARATOR
- label
- Not enrolled in group therapy
- description
- Patients in control arm will be issued surveys
- interventionNames
- Other: Surveys
Primary outcomes (2)
- measure
- Assessment of MAX-PC Scores
- timeFrame
- Change from baseline to 4 weeks to 12 weeks
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 40 Years
Show eligibility criteria text
Inclusion Criteria: * Age of 40 * Primary diagnosis of Prostate Cancer * Initial MAX-PC score of ≥16. * Sign a consent form allowing related information to be included in this research. Exclusion Criteria: * Prostate cancer is not their primary diagnosis. * Have pre-existing diagnosed psychiatric conditions, are currently taking psychotropic medications (e.g., antidepressants, anxiolytics, mood stabilizers.) * Have been diagnosed with cancer other than prostate cancer (and non-melanoma skin cancer) * Evidence of active substance abuse. * Participants in the treatment group who are absent from more than 3 therapy sessions will be excluded.
References
Publications (0)
Data not yet available