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Group Visits for Patients with Enlarges Prostates: Enhancing Patient Care, Cutting Wait Times – Evidence from a Study Comparing Shared Appointments to One-on-One Sessions.

Phase 3
Conditions
Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
Registration Number
CTRI/2024/01/061605
Lead Sponsor
Priyank Yadav
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

We will have the following inclusion criteria:

1. The patient must be 50 years or older.

2. The patient must have regular visits at Urology Clinic in SGPGIMS.

3. The patients should have come for follow up visits only, requiring no examination.

4. The patient should not have any symptoms requiring admission or any procedure with or without anaesthesia.

5. International Prostate Symptom Score (IPSS) of eight or more.

6. The patient should not require surgical intervention in the near future.

7. The patient must not wish to interact with a specific doctor.

Exclusion Criteria

We will have the following exclusion criteria:

1. Any physical or mental conditions in the patient or accompanying persons that preclude interaction in a group setting.

2. Participation of the patient in any other existing trial.

3. The patient had not indwelling catheters, urinary incontinence, anuria, gross haematuria, acute urinary retention, urinary tract infection, and prostate cancer.

4. Any patient who needs clinical examination will be excluded for reasons of privacy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Patient waiting time <br/ ><br>2. Patient consultation timeTimepoint: All primary outcomes will be measured at 0 and 6 months
Secondary Outcome Measures
NameTimeMethod
1. Patient anxiety <br/ ><br>2. Patient knowledge <br/ ><br>3. Patient satisfaction <br/ ><br>4. Engagement in SMA <br/ ><br>5. Doctor’s productivity <br/ ><br>Timepoint: Secondary outcome will be measured at 0 and 6 months
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