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To see the effect of Tata mini quality of questionnaire on patients needs in hospital

A Prospective Randomised trial to assess clinical utility of the TMH Mini Quality of Life (TMQ) questionnaire. - TMQ

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022442
Enrollment
642
Registered
2019-12-18
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: C50-C50- Malignant neoplasms of breast Health Condition 2: C15-C26- Malignant neoplasms of digestive organs Health Condition 3: C51-C58- Malignant neoplasms of female genital organs Health Condition 4: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx Health Condition 5: C30-C39- Malignant neoplasms of respiratory and intrathoracic organs

Interventions

Intervention1: TMQ Questionnaire: Patient fills TMQ questionnaire which is clipped to the file before OPD consultation Control Intervention1: OPD CONSULTATION: Patient procceds for OPD consultation w

Sponsors

Tata Memorial Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: age greater than 18 sex both patient can read site head and neck, breast, gynaecology, thoracic, gastrointestinal reveiving curative or pallaiative treatment or on follow up KPS greater than 50% No history of major psychiatrist illness

Exclusion criteria

Exclusion criteria: nil

Design outcomes

Primary

MeasureTime frame
Differences in the two randomized groups in terms of the EMR documentation and redressal of issues that may be affecting a patientâ??s Health Related QoL.Timepoint: 48 hours after opd consultation—

Secondary

MeasureTime frame
Correlation between the documentation and redressal rates of QoL issues reported by patients and the patients self-reported scores (from 1 to 4) in the test arm Measurement ofTimepoint: 48 hours after opd consultation;Difference in patient satisfaction with the consultation between the two randomized groups. (measure of utility)Timepoint: 48 hours after opd consultation;Differences between documentation and redressal rates of QoL issues reported by patients in the two randomized groups with respect to a. Curative versus palliative intent of treatment b. Patients on active treatment versus on follow-up c. Patients registered as â??generalâ?? versus â??privateâ??Timepoint: 48 hours after opd consultation—

Countries

India

Contacts

Public ContactDr Rajiv Sarin

Tata Memorial Hospital

drrajivsarin@gmail.com9820313789

Outcome results

None listed

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