Clinical trial · Observational
Feasibility Study Of A Telephonic Questionnaire For Follow-Up Of Locally Advanced Cervical Cancer Patients
A Cross-Sectional Feasibility Study of a Telephonic Questionnaire By Research Nurses For Follow-Up Of Locally Advanced Cervical Cancer Patients With Complete Response To Treatment.
NCT03477240CI-TRIAL-00032232unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Cross-sectional Feasibility study on all consecutive patients of locally advanced cancer of the cervix or vault treated entirely at Tata Memorial Centre with curative intent radiation or chemoradiation.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer Stage IIIB | Malignant Cervical Neoplasm | CURATED_BROADER | 0.78 |
| Follow up | — | UNRESOLVED | — |
| QUESTIONNAIRE | — | UNRESOLVED | — |
| Treatment Outcome | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Accuracy of nurse-led telephonic interview for disease recurrence
- timeFrame
- 1 YEAR
- description
- To estimate the accuracy of nurse-led telephonic interview in identifying patients with symptoms suggestive of disease recurrence, in terms of sensitivity and specificity values
Secondary outcomes (2)
- measure
- Accuracy of nurse-led telephonic interview for late toxicity of treatment
- timeFrame
- 1 YEAR
- description
- To estimate the accuracy of nurse-led telephonic interview in identifying patients with symptoms suggestive of late toxicity of treatment
- measure
- Acceptability of a nurse-led telephonic surveillance program using structured format (Form C).
- timeFrame
- 1 YEAR
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
Show eligibility criteria text
Inclusion Criteria: 1. Cervical Cancer Stage Ib2, II and III (Squamous carcinoma or adenocarcinoma) 2. Cancer of the vault 3. Cancer of the cervix which inadvertently underwent hysterectomy (inadequate surgery) 4. Treated with curative intent with radical radio(chemo)therapy or NACT followed by radical radio(chemo)therapy and completed all curative treatment. 5. Within 2 years post completion of treatment 6. Has complete clinical response at 3 months post treatment 7. Informed consent 8. Contactable by telephone Exclusion Criteria: 1. Patients with Stage III disease treated with palliative intent with once monthly radiotherapy 2. Early stage cervical cancer patients who underwent Wertheims hysterectomy and who have completed adjuvant radiochemotherapy due to high-risk factors 3. Metastatic cervical cancers 4. Patients who are unable to comprehend the questions or dialogue over telephone by medical staff. 5. Patients who seem unreliable for follow up
References
Publications (0)
Data not yet available
No reference posted for this study.