Skip to content

A Multicenter Cross-Sectional Survey in India to Assess Patient Experiences, Barriers, and Unmet Needs Among Patients with Prostate Cancer.

Prostate Cancer Patient Experience and Outcomes Survey (P-PEOS):A Multicenter Cross-Sectional Assessment of Patient-Reported Experiences,Barriers,and Unmet Needs in India. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/106817
Enrollment
800
Registered
2026-03-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C61- Malignant neoplasm of prostate

Interventions

Intervention1: Nil: Nil

Sponsors

Mahamana Pandit Madan Mohan Malaviya Cancer Centre (MPMMCC)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male gender aged 18 years or above 2.Histologically confirmed diagnosis of adenocarcinoma of the prostate at any stage 3.Currently receiving active treatment by any modality or on follow up after primary treatment 4.Able to understand the study information and provide written informed consent in a locally understood language 5.Able to complete the questionnaire independently or with minimal non leading assistance from a trained study coordinator or caregiver

Exclusion criteria

Exclusion criteria: 1.Any cognitive impairment or psychiatric condition that, in the opinion of the treating physician, would preclude meaningful participation in the survey. 2.Patients who are critically ill or hospitalized in an unstable condition at the time of approach.

Design outcomes

Primary

MeasureTime frame
Primary ObjectiveTo evaluate patient-reported experiences, symptom burden, health-related quality of life (HRQoL), factors influencing treatment decision-making, and perceived gaps in care delivery among men diagnosed with prostate cancer in India.Timepoint: 2 years

Secondary

MeasureTime frame
1.To identify and quantify delays in the diagnostic pathway and treatment initiation. 2.To characterize patient-reported toxicities associated with different treatment modalities (e.g., surgery, radiation, ADT, novel hormonal agents, chemotherapy). 3.To assess the prevalence and severity of financial toxicity and the associated travel burden. 4.To evaluate psychological health (anxiety and depression) and sexual health concerns. 5.To assess patient awareness and perceptions regarding clinical trials, advanced diagnostics (e.g. PSMA PET) and novel treatments. 6.To measure digital health readiness, including comfort with technology and acceptance of telemedicine. 7.To identify key unmet needs and patient priorities to inform national clinical practice guidelines and patient support programs. Timepoint: 2 years

Countries

India

Contacts

Public ContactDr Arpita Singh

Mahamana Pandit Madanmohan Malviya Cancer Centre (MPMMCC)

singh.arpita0911@gmail.com7394071818

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026