Trial Outcomes & Findings for The Personal Patient Profile Decision Support for Patients With Bladder Cancer (NCT NCT05033067)

NCT ID: NCT05033067

Last Updated: 2026-04-24

Results Overview

Investigator-designed 12-items instrument to evaluate intervention participants' opinions and acceptance of study procedures and their satisfaction with the decisional aid. Responses for each item range from strongly agree (1) to strongly disagree (4), with higher scores indicating greater dissatisfaction with the intervention. Original responses (1-5 visual analogue scale) were categorized as Low (scores 1-2), Neutral (score 3), or High (scores 4-5). with higher scores indicating greater dissatisfaction with the intervention.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

24 participants

Primary outcome timeframe

1 month follow-up

Results posted on

2026-04-24

Participant Flow

After obtaining IRB approval for the feasibility study, we approached 114 patients for recruitment into The Personal Patient Profile Decision Support for Patients with Bladder Cancer (P3-BC) study. Of these, 24 patients consented to participate. Common reasons for declining included disease and treatment burden, limited time, and lack of confidence in using technology independently.

Among those who consented, 4 participants were lost to follow-up prior to participation, leaving 20 participants (83%) who engaged with the web-based tool's survey. Of these, 5 participants did not complete sufficient baseline survey engagement (i.e., completing the tool's survey that precedes the randomization step) with the tool and were therefore not assigned to a study group. The remaining 15 participants were randomized, with 10 assigned to the intervention group and 5 to the usual care.

Participant milestones

Participant milestones
Measure
Participants With Bladder Cancer
Participants who consented to participate in the study and were offered to engage with the web-based tool's survey.
Intervention (P3-BC) Usual Care
In addition to receiving usual care, patients had access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Usual Care
Usual Care Control Group - The group received standard bladder cancer care information only.
Consented, engaged with web-based tool
STARTED
24
0
0
Consented, engaged with web-based tool
COMPLETED
15
0
0
Consented, engaged with web-based tool
NOT COMPLETED
9
0
0
Randomization
STARTED
0
10
5
Randomization
COMPLETED
0
8
3
Randomization
NOT COMPLETED
0
2
2

Reasons for withdrawal

Reasons for withdrawal
Measure
Participants With Bladder Cancer
Participants who consented to participate in the study and were offered to engage with the web-based tool's survey.
Intervention (P3-BC) Usual Care
In addition to receiving usual care, patients had access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Usual Care
Usual Care Control Group - The group received standard bladder cancer care information only.
Consented, engaged with web-based tool
Lost to Follow-up
4
0
0
Consented, engaged with web-based tool
baseline survey not completed
5
0
0
Randomization
Withdrawal by Subject
0
1
1
Randomization
Lost to Follow-up
0
1
1

Baseline Characteristics

The Personal Patient Profile Decision Support for Patients With Bladder Cancer

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Intervention (P3-BC) Care
n=10 Participants
In addition to receiving usual care, patients had access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Usual Care
n=5 Participants
Usual Care Control Arm - The group received standard bladder cancer care information only.
Total
n=15 Participants
Total of all reporting groups
Age, Continuous
67.9 years
STANDARD_DEVIATION 3.1 • n=2 Participants
79.8 years
STANDARD_DEVIATION 4.1 • n=1 Participants
70.1 years
STANDARD_DEVIATION 7.1 • n=3 Participants
Sex: Female, Male
Female
1 Participants
n=2 Participants
2 Participants
n=1 Participants
3 Participants
n=3 Participants
Sex: Female, Male
Male
9 Participants
n=2 Participants
3 Participants
n=1 Participants
12 Participants
n=3 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=2 Participants
0 Participants
n=1 Participants
0 Participants
n=3 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
10 Participants
n=2 Participants
5 Participants
n=1 Participants
15 Participants
n=3 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=2 Participants
0 Participants
n=1 Participants
0 Participants
n=3 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=2 Participants
0 Participants
n=1 Participants
0 Participants
n=3 Participants
Race (NIH/OMB)
Asian
0 Participants
n=2 Participants
1 Participants
n=1 Participants
1 Participants
n=3 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=2 Participants
0 Participants
n=1 Participants
0 Participants
n=3 Participants
Race (NIH/OMB)
Black or African American
1 Participants
n=2 Participants
0 Participants
n=1 Participants
1 Participants
n=3 Participants
Race (NIH/OMB)
White
9 Participants
n=2 Participants
4 Participants
n=1 Participants
13 Participants
n=3 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=2 Participants
0 Participants
n=1 Participants
0 Participants
n=3 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=2 Participants
0 Participants
n=1 Participants
0 Participants
n=3 Participants
Number of Participants with Heart Disease
1 Participants
n=2 Participants
1 Participants
n=1 Participants
2 Participants
n=3 Participants
Number of participants with Diabetes
5 Participants
n=2 Participants
1 Participants
n=1 Participants
6 Participants
n=3 Participants
Number of Participants with Peripheral Neuropathy
1 Participants
n=2 Participants
0 Participants
n=1 Participants
1 Participants
n=3 Participants
Number of participants with Chronic Kidney disease
1 Participants
n=2 Participants
0 Participants
n=1 Participants
1 Participants
n=3 Participants

PRIMARY outcome

Timeframe: 1 month Follow-up

Population: Data for participants who took the survey and thus randomized to the intervention group.

Percentage of participants who agreed with the statements taken from the Survey-based Acceptability Measure Acceptability is assessed with the 13-item web-based scale in addition to items designed by the research team for the 1-month follow-up to evaluate acceptability. The acceptability is defined as 80% acceptable ratings. Using well-established feasibility criteria to assess: 1) retention/drop-out rates, and 2) duration and completion rate of study assessments. The scale uses a 5-point response scale for each item (1=not acceptable, 5=highly acceptable). Responses were categorized to agree (scores 1-2 strongly agree/agree), or disagree (scores 3-5; strongly disagree, disagree, I don't know.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=8 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Percent of Participants Who Agree Using the Acceptability Scale
Helped me make my treatment decisions
71.4 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Increased my knowledge about my treatment (diversion options)
62.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Sort out what's important to me for decision making
62.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Taught me how to use stoma appliances or catheters
62.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Helped me manage my disease
50.0 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Prepared me for the surgery side effects
37.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Made me feel less anxious or upset about my treatment
62.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Taught me how to care for myself after surgery
62.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Helped me reduce my anxiety about my treatment
62.5 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Helped me talk to doctors about my treatment options
50.0 percentage of participants
Percent of Participants Who Agree Using the Acceptability Scale
Helped me take care of myself
50.0 percentage of participants

PRIMARY outcome

Timeframe: 1 month followup

Population: In addition to receiving usual care, participants had access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.Data for participants who took the survey and thus randomized to the intervention group.

A 1-month follow-up questionnaire included 11 additional items assessing participants' perceptions of study procedures, acceptance of the intervention, and satisfaction with the decision aid. Responses were categorized to agree (scores 1-2 strongly agree/agree), or disagree (scores 3-5; strongly disagree, disagree, I don't know).

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=8 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=8 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Helped me take care of myself
4 Participants
4 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Helped me reduce my anxiety about my treatment
5 Participants
3 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Helped me talk to doctors about my treatment options
4 Participants
4 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Helped me manage my disease
4 Participants
4 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Prepared me for the surgery side effects
4 Participants
4 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Taught me how to use stoma appliances or catheters
5 Participants
3 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Taught me how to care for myself after surgery
5 Participants
3 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Increased my knowledge about my treatment (diversion options)
5 Participants
3 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Made me feel less anxious or upset about my treatment
5 Participants
3 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Sort out what's important to me for decision making
5 Participants
3 Participants
Number of Participants Who Agree or Disagree With Statements on the Acceptability E-scale
Helped me make my treatment decisions
6 Participants
2 Participants

PRIMARY outcome

Timeframe: 1 month follow-up

Population: Data collected for participants who completed the web-based survey. Some participants did not reply to each item. These participants, in addition to receiving usual care, patients had access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.

Investigator-designed 12-items instrument to evaluate intervention participants' opinions and acceptance of study procedures and their satisfaction with the decisional aid. Responses for each item range from strongly agree (1) to strongly disagree (4), with higher scores indicating greater dissatisfaction with the intervention. Original responses (1-5 visual analogue scale) were categorized as Low (scores 1-2), Neutral (score 3), or High (scores 4-5). with higher scores indicating greater dissatisfaction with the intervention.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=10 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=10 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
n=10 Participants
1-5 visual analogue scale - scores 4-5
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
How understandable were the questions?
0 percent of participants
0 percent of participants
100 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
How easy was the program to use?
0 percent of participants
14 percent of participants
86 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Overall satisfaction with the program
0 percent of participants
14 percent of participants
86 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Usefulness of information on statistics
14 percent of participants
0 percent of participants
86 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Was the amount of time to complete the program acceptable?
0 percent of participants
29 percent of participants
71 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Usefulness of information about top concerns
28 percent of participants
14 percent of participants
58 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
How helpful was it to complete the program?
14 percent of participants
29 percent of participants
57 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
How valuable was the information?
14 percent of participants
14 percent of participants
72 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Usefulness of videos
14 percent of participants
29 percent of participants
57 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Usefulness of links to bladder cancer websites
0 percent of participants
17 percent of participants
83 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Usefulness of examples of what to say to your doctor
28 percent of participants
29 percent of participants
43 percent of participants
Percent of Participants Agreeing or Disagreeing With the Decision Using the Program Evaluation Scale
Usefulness of information on role in decision-making
14 percent of participants
29 percent of participants
57 percent of participants

SECONDARY outcome

Timeframe: 1 month follow-up

Population: One participant did not complete the 1 month follow up survey.

Shared decision making (SDM) was assessed by the SDMQ-9. The 9 items are rated on a 6-point Likert scale ranging from 0 (completely disagree) to 5 (completely agree). Final scores are sum of rating, which ranges between 0 and 45, higher score indicates more positive attitude towards SDM.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=10 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=4 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Shared Decision Making Questionnaire (SDM-Q-9)
5.43 score on a scale
Standard Deviation 0.54
5.47 score on a scale
Standard Deviation 0.42

SECONDARY outcome

Timeframe: 3 months follow-up

Consists of 16 item scale measuring effectiveness on decision making. Items are given a score value of 0 = strongly agree, 1 = agree, 2 = neither agree nor disagree, 3= disagree, and 4 = disagree, full scale from 0 - 64 with higher total scores indicating higher decisional conflict.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=8 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=3 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Decisional Conflict Scale
4.28 score on a scale
Standard Deviation 0.39
4.56 score on a scale
Standard Deviation 0.39

SECONDARY outcome

Timeframe: 1 month follow-up and 3 month follow-up

Brief Symptom Index (BSI-18) was used psychological to assess distress. BSI-18 is a self-report 18-item instrument. Index full scale is scored .00 to 0.94 with higher scores indicating more distress.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=8 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=3 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Brief Symptom Index (BSI-18)
1 month follow up
0.51 score on a scale
Standard Deviation 0.73
0.15 score on a scale
Standard Deviation 0.21
Brief Symptom Index (BSI-18)
3 months follow up
0.26 score on a scale
Standard Deviation 0.32
0.07 score on a scale
Standard Deviation 0.08

SECONDARY outcome

Timeframe: 3 months follow-up

The Decisional Regret Scale consists of 5 item scale assessing regret of treatment decisions made. Each item scored from 1 to 5. Full scale is scored 1-25. Higher score indicates higher regret of treatment decisions.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=8 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=3 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Decisional Regret Scale
4.38 score on a scale
Standard Deviation 0.59
4.67 score on a scale
Standard Deviation 0.42

SECONDARY outcome

Timeframe: 1 month follow-up

The Cancer Rehabilitation Evaluation System (CARES-MIS) - Medical Interaction Subscale was used to assess perceived problems with communication with providers. The CARES - Medical Interaction Subscale includes 11 items rated on 5-point scale, where 0 represents "not at all" and 4 represents that problem occurred "very much". Total scores range from 0-44 for The CARES-MIS. 5 items were selected from The CARES-MIS, total subscale score range is 0-20, with higher scores indicating poorer perceived communication

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 3 months follow-up

Population: Data available for participants who completed the survey

A 14 investigator-designed items evaluating patients' knowledge about bladder cancer. Scores range from 1 (Completely certain that is true) to 5 (Completely certain that is false). After recording the items to 1 (true) and 0 (false) total sum score of this scale range from 0 -14, with higher scores indicating more knowledge about bladder cancer.

Outcome measures

Outcome measures
Measure
Intervention (P3-BC) Usual Care
n=8 Participants
In addition to receiving usual care, patients will have access to the aid and related materials before consultation with the physician about cystectomy and urinary diversion.
Disagree
n=3 Participants
(scores 3-5; strongly disagree, disagree, I don't know)
High (4-5)
1-5 visual analogue scale - scores 4-5
Bladder Cancer Knowledge Scale
11.1250 score on a scale
Standard Deviation 2.10
11.333 score on a scale
Standard Deviation 0.58

Adverse Events

Intervention (P3-BC) Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Usual Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Nihal Mohamed, PhD

Icahn School of Medicine at Mount Sinai

Phone: (212) 241-8858

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place