Unveiling Patient Experiences in Testicular Cancer Clinical Trials
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT05928377 |
Recruitment Status :
Not yet recruiting
First Posted : July 3, 2023
Last Update Posted : July 3, 2023
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Clinical research participation has historically been heavily biased toward specific demographics.
Several people will be invited to enroll in this study so that it may collect a variety of data about testicular cancer clinical study experiences and identify barriers to participation as well as the causes of participants' failure or withdrawal.
People with testicular cancer who are invited to take part in medical research will benefit from the analysis of the data.
Condition or disease |
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Testicular Cancer |
Study Type : | Observational |
Estimated Enrollment : | 500 participants |
Observational Model: | Case-Crossover |
Time Perspective: | Prospective |
Official Title: | Patient Perspectives in Testicular Cancer Clinical Trials: Insights Into Participating in Studies for Testicular Cancer |
Estimated Study Start Date : | July 2024 |
Estimated Primary Completion Date : | July 2025 |
Estimated Study Completion Date : | July 2026 |
- Number of testicular cancer patients who decide to enroll in a clinical trial [ Time Frame: 3 months ]
- Rate of testicular cancer patients who remain in a clinical trial to trial completion [ Time Frame: 12 months ]
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | Male |
Gender Based Eligibility: | Yes |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Inclusion Criteria:
- Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
- Diagnosis of testicular cancer
- No prior treatment for testicular cancer
Exclusion Criteria:
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
- Enrolled in another research study
- Inability to provide written informed consent
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05928377
Contact: Michael B Gill | 4159004227 | bask@withpower.com |
United States, California | |
Power Life Sciences | |
San Francisco, California, United States, 94107 |
Study Director: | Michael B Gill | Power Life Sciences Inc. |
Responsible Party: | Power Life Sciences Inc. |
ClinicalTrials.gov Identifier: | NCT05928377 |
Other Study ID Numbers: |
80505443 |
First Posted: | July 3, 2023 Key Record Dates |
Last Update Posted: | July 3, 2023 |
Last Verified: | June 2023 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
testicular cancer |
Testicular Neoplasms Endocrine Gland Neoplasms Neoplasms by Site Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Genital Diseases, Male |
Genital Diseases Urogenital Diseases Male Urogenital Diseases Endocrine System Diseases Testicular Diseases Gonadal Disorders |