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Distress Evaluation in Survivor of Cervical Cancer

Evaluation of Distress in Survivor of Cervical Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/02/031110
Enrollment
2000
Registered
2021-02-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified

Interventions

None listed

Sponsors

Tata Memorial Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with cervical cancer and treated with radical intent 2.Age more than 18yrs. 3.Patients who have completed at least 6 months of follow up 4.Patients which are known to be disease free at the time of study 5. Well versed with Hindi, Marathi or English language

Exclusion criteria

Exclusion criteria: 1.Refusal to give informed consent. 2.Metastatic disease at the presentation. 3.Prior history of any psychiatric illness or currently receiving anti-psychotic drugs. 4.Patients with relapse

Design outcomes

Primary

MeasureTime frame
Prevalence of distress in cervix cancer survivorsTimepoint: During follow-up visits (minimum 6 months)

Secondary

MeasureTime frame
Causes of distress in cervical cancer survivalTimepoint: During follow-up visits (minimum 6 months)

Countries

India

Contacts

Public ContactDr Gayatri Patil

Advanced Centre for Treatment, Research and Education in Cancer (ACTREC)

supriyasastri@gmail.com9930958309

Outcome results

None listed

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