Advanced Prostate CarcinomaWATappNCT04851639
The Wolverhampton Assessment Tool, a Tool for Patient-reported Wellbeing in the Context of Prostate Cancer
A study testing Wolverhampton Assessment Tool in people with Advanced Prostate Carcinoma, run by University of Wolverhampton at 1 site in United Kingdom.
Trial summary
This is a study of the Wolverhampton Assessment Tool (WATapp), a five-item questionnaire for patients with advanced or metastatic prostate cancer to say how they feel normally in terms of pain, urinary frequency, eating, and tiredness. Read more about this study
- Who is it for?
- Any age, men only
- Conditions the study is for
- Advanced Prostate Carcinoma
- What is being tested?
- Wolverhampton Assessment Tool
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 1 Sep 2020to 30 Mar 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Men only
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- born male
- diagnosed with advanced or metastatic prostate cancer
- able to read and speak English
Who cannot join
- not born male
- not diagnosed with advanced or metastatic prostate cancer
- not able to read and speak English
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site, 1 recruiting
- Recruiting
Royal Wolverhampton Hospital NHS Trust
Wolverhampton, WV10 0QP
Ian Sayers, MBBS, 07789935567, iansayers@nhs.net
About this study
Official title: The Wolverhampton Assessment Tool, a Step Towards Remote Monitoring of Patient-reported Wellbeing in the Context of Prostate Cancer
This is a study of the Wolverhampton Assessment Tool (WATapp), a five-item questionnaire for patients with advanced or metastatic prostate cancer to say how they feel normally in terms of pain, urinary frequency, eating, and tiredness. It is widely recognised that patient-reported outcomes give a measure of overall effect of clinicians' actions on patients and that they can be used to guide the management of the patient's condition.
WATapp is designed to reduce the need for the patient to attend hospital so much for routine follow-up consultations (an important aspect in light of COVID-19), to give the patient some sense of agency and control and to inform his clinician of just he feels he is coping with his treatment. Now the investigators want to find out just how the results from WATapp correspond to, for example, changes in the patient's PSA, testosterone or other blood results which are routinely measured; and to find out how patients and clinicians feel about using WATapp.
Men with advanced or metastatic prostate cancer will be eligible to take part in the study and participation is in addition to whatever treatment they are on. Clinicians who choose to offer WATapp to their patients will also be invited to take part and they will be asked to share with the researchers anonymised, linked patient data and scores from WATapp.
Read the detailed description
It is widely recognised that patient-reported outcomes give a measure of overall effect of clinicians' actions on patients and that they can be used to guide the management of the patient's condition. They can also have an empowering effect as the patient may feel that they are agents, and not just subjects, in their treatment pathway. In the case of advanced and metastatic prostate cancer (i.e. cancer which has spread from the prostate to distant sites), the clinical means of assessing how the patient's disease is responding to treatment (radiological/magnetic scans) are somewhat imperfect as they do not take into account the impact on the patient's life and his response and reaction. Patient-reported outcomes, such as WATapp, allow a way to measure the impact of clinicians' actions on patients' lives. They offer an assessment of how well treatments are working and this is critical in the management of patients with advanced or metastatic prostate cancer. Failure to recognise how the patient responds to treatment can lead to effective treatment being stopped inappropriately; progression of the disease may not always be recognised; and the patient may have unnecessary side effects that go unchecked. Ignoring the patient-reported outcomes, such as WATapp, can reduce the opportunity to use alternative treatments. WATapp has been developed as an objective and reproducible clinical assessment tool by using questions from these validated clinical study tools:
The Functional Assessment of Cancer Therapy - Prostate; The Brief Pain Inventory; The Karnofsky Performance Scale
WATapp was refined with patient and clinician input to produced the present 5-item questionnaire.
This is a mixed-method study, incorporating both quantitative and qualitative elements. As such, it is both objective and subjective:
- It is subjective in that, in using the WATapp, the patient selects his response to each question on the basis of how he feels normally
- It is objective in that the tools to be used in the analysis of the quantitative data [i.e. statistical tests such as Mann Whitney-U, Spearman Rank Correlation etc.] are independent of the person using them
- Determining clinically the patient's disease status employs objective measures such as PSA, size, distribution and type of metastasis, frequency of night-time urination etc. as well as the clinician's professional judgment which contains both objective and subjective elements
- The researchers are not mirrors but rather prisms and hence the entire study from conception to analysis and report is a refraction of their experiences
Phase 1 The main outcome of the first phase will be to refine, as necessary, both the WATapp and the research instruments as well as to establish proof of principle of the clinical utility of WATapp. This will entail a full pilot of the WATapp in New Cross Hospital, Wolverhampton. Patients who agree to use the WATapp to self-monitor aspects of their health will be invited to consent to share with the researchers their anonymised data from it as well as linked, anonymised clinical data. The frequency of collection of data will be at the discretion of the clinician. Participating patients and clinicians will be invited to take part in a short, semi-structured interview on their experience of using WATapp. All patient data will be treated anonymously, and none linked back to the patient or to their clinician/s. Clinicians will be asked to record any reasons given by patients who decline to use the WATapp. Whether a patient chooses or not to use WATapp or chooses or not to take part in this study will have no bearing on their clinical care.
The clinical data sought on patients will include:
- Age
- Stage of cancer at diagnosis in terms of the primary tumour, and any presence of disease in lymph nodes and bones
- Current stage of cancer in terms of the primary tumour, and any presence of disease in lymph nodes and bones
- Level of PSA - prostate specific antigen, produced normally in the prostate but also produced in prostate cancer cells, testosterone and other blood results which are routinely measured
- Any other illnesses the patient may have
- Current and previous treatments
Phase 2 The second phase is to invite oncologists across the West Midlands of England, many of whom have already expressed an interest, to join the study and to send the researchers anonymised, linked patient data (as in Phase 1) and that from the WATapp.
- Conditions
- Advanced Prostate Carcinoma
- Being tested
- Wolverhampton Assessment Tool
- Keywords
- metastatic, quality of life, patient empowerment
- Medical subject headings
- Neoplasm Metastasis, Patient Participation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Wolverhampton Assessment ToolOther
a proxy means for assessing whether clinician intervention is required and to assess patient's lived quality of life
| Study group | Role | What they receive |
|---|---|---|
| Proof of principle | Experimental | Proof of principle of the efficacy and utility of the WATapp Receives: Other: Wolverhampton Assessment Tool |
What is being measured
The primary outcome is the main question the study is designed to answer.
WATapp as a proxy for patients' clinical status
The correlation between the patient's responses to WATapp and their clinical status as measured by routine bloods and clinician assessment.
Measured: up to 48 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Apr 2021
- Study start1 Sep 2020
- Primary completion30 Sep 2024 (estimated)
- Study completion30 Mar 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Advanced Prostate CarcinomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- any patient with advanced or metastatic prostate cancer
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Wolverhampton
- Sponsor type
- University, hospital or other
- Collaborators
- The Royal Wolverhampton Hospitals NHS Trust
- Responsible party
- Principal investigator, Dr David Matheson, University of Wolverhampton
- Investigators
- David Matheson, PhD, Principal investigator, University of Wolverhampton
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04851639
- Sponsor's protocol ID
- 284454
- Acronym
- WATapp
- Status last verified
- Sep 2021
- First submitted
- 6 Apr 2021
- Last updated
- 5 Oct 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The IPD plan is in development. It is expected that it will include * Study protocol * Information sheets and blank informed consent forms * Anonymised data from the study Sharing will be subject to application, guarantees as to usage, due recognition of source
Study at a glance
From the registry record, last updated by the sponsor on 5 Oct 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Wolverhampton Assessment Tool, a Step Towards Remote Monitoring of Patient-reported Wellbeing in the Context of Prostate Cancer
- ClinicalTrials.gov ID
- NCT04851639
- Acronym / sponsor ID
- WATapp / 284454
- Conditions
- Advanced Prostate Carcinoma
- Keywords
- metastatic, quality of life, patient empowerment
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- University of WolverhamptonUniversity, hospital or other
- Collaborators
- The Royal Wolverhampton Hospitals NHS Trust
- Study start
- 1 Sep 2020 (actual)
- Primary completion
- 30 Sep 2024 (estimated)
- Study completion
- 30 Mar 2025 (estimated)
- First posted
- 20 Apr 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a study of the Wolverhampton Assessment Tool (WATapp), a five-item questionnaire for patients with advanced or metastatic prostate cancer to say how they feel normally in terms of pain, urinary frequency, eating, and tiredness. It is widely recognised that patient-reported outcomes give a measure of overall effect of clinicians' actions on patients and that they can be used to guide the management of the patient's condition.
WATapp is designed to reduce the need for the patient to attend hospital so much for routine follow-up consultations (an important aspect in light of COVID-19), to give the patient some sense of agency and control and to inform his clinician of just he feels he is coping with his treatment. Now the investigators want to find out just how the results from WATapp correspond to, for example, changes in the patient's PSA, testosterone or other blood results which are routinely measured; and to find out how patients and clinicians feel about using WATapp.
Men with advanced or metastatic prostate cancer will be eligible to take part in the study and participation is in addition to whatever treatment they are on. Clinicians who choose to offer WATapp to their patients will also be invited to take part and they will be asked to share with the researchers anonymised, linked patient data and scores from WATapp.
Detailed description
It is widely recognised that patient-reported outcomes give a measure of overall effect of clinicians' actions on patients and that they can be used to guide the management of the patient's condition. They can also have an empowering effect as the patient may feel that they are agents, and not just subjects, in their treatment pathway. In the case of advanced and metastatic prostate cancer (i.e. cancer which has spread from the prostate to distant sites), the clinical means of assessing how the patient's disease is responding to treatment (radiological/magnetic scans) are somewhat imperfect as they do not take into account the impact on the patient's life and his response and reaction. Patient-reported outcomes, such as WATapp, allow a way to measure the impact of clinicians' actions on patients' lives. They offer an assessment of how well treatments are working and this is critical in the management of patients with advanced or metastatic prostate cancer. Failure to recognise how the patient responds to treatment can lead to effective treatment being stopped inappropriately; progression of the disease may not always be recognised; and the patient may have unnecessary side effects that go unchecked. Ignoring the patient-reported outcomes, such as WATapp, can reduce the opportunity to use alternative treatments. WATapp has been developed as an objective and reproducible clinical assessment tool by using questions from these validated clinical study tools:
The Functional Assessment of Cancer Therapy - Prostate; The Brief Pain Inventory; The Karnofsky Performance Scale
WATapp was refined with patient and clinician input to produced the present 5-item questionnaire.
This is a mixed-method study, incorporating both quantitative and qualitative elements. As such, it is both objective and subjective:
- It is subjective in that, in using the WATapp, the patient selects his response to each question on the basis of how he feels normally
- It is objective in that the tools to be used in the analysis of the quantitative data [i.e. statistical tests such as Mann Whitney-U, Spearman Rank Correlation etc.] are independent of the person using them
- Determining clinically the patient's disease status employs objective measures such as PSA, size, distribution and type of metastasis, frequency of night-time urination etc. as well as the clinician's professional judgment which contains both objective and subjective elements
- The researchers are not mirrors but rather prisms and hence the entire study from conception to analysis and report is a refraction of their experiences
Phase 1 The main outcome of the first phase will be to refine, as necessary, both the WATapp and the research instruments as well as to establish proof of principle of the clinical utility of WATapp. This will entail a full pilot of the WATapp in New Cross Hospital, Wolverhampton. Patients who agree to use the WATapp to self-monitor aspects of their health will be invited to consent to share with the researchers their anonymised data from it as well as linked, anonymised clinical data. The frequency of collection of data will be at the discretion of the clinician. Participating patients and clinicians will be invited to take part in a short, semi-structured interview on their experience of using WATapp. All patient data will be treated anonymously, and none linked back to the patient or to their clinician/s. Clinicians will be asked to record any reasons given by patients who decline to use the WATapp. Whether a patient chooses or not to use WATapp or chooses or not to take part in this study will have no bearing on their clinical care.
The clinical data sought on patients will include:
- Age
- Stage of cancer at diagnosis in terms of the primary tumour, and any presence of disease in lymph nodes and bones
- Current stage of cancer in terms of the primary tumour, and any presence of disease in lymph nodes and bones
- Level of PSA - prostate specific antigen, produced normally in the prostate but also produced in prostate cancer cells, testosterone and other blood results which are routinely measured
- Any other illnesses the patient may have
- Current and previous treatments
Phase 2 The second phase is to invite oncologists across the West Midlands of England, many of whom have already expressed an interest, to join the study and to send the researchers anonymised, linked patient data (as in Phase 1) and that from the WATapp.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- any patient with advanced or metastatic prostate cancer
| Arm | Type | Receives |
|---|---|---|
| Proof of principle | Experimental | Other: Wolverhampton Assessment ToolProof of principle of the efficacy and utility of the WATapp |
Who may qualify
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- born male
- diagnosed with advanced or metastatic prostate cancer
- able to read and speak English
Key exclusion criteria (3 listed)
- not born male
- not diagnosed with advanced or metastatic prostate cancer
- not able to read and speak English
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Wolverhampton Assessment Toola proxy means for assessing whether clinician intervention is required and to assess patient's lived quality of life | Other | Proof of principle |
Primary outcome
WATapp as a proxy for patients' clinical status
Time frame: up to 48 months
The correlation between the patient's responses to WATapp and their clinical status as measured by routine bloods and clinician assessment.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Oct 2021.
- Individual participant dataSharing planned: Yes. The IPD plan is in development. It is expected that it will include * Study protocol * Information sheets and blank informed consent forms * Anonymised data from the study Sharing will be subject to application, guarantees as to usage, due recognition of source
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
David Matheson, PhD principal investigator
University of Wolverhampton
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Wolverhampton Assessment Tool in people with Advanced Prostate Carcinoma, run by University of Wolverhampton at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 5 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact David Matheson, PhD (+447469882072, d.matheson@wlv.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
WATapp as a proxy for patients' clinical status (time frame: up to 48 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Oct 2021; AzTrials last refreshed its copy on 30 Oct 2026.