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A study on cancer patients receiving chemotherapy to identify the occurrence of depression in those cancer patients using questionnaire tools.

Assessment of Prevalence of Depression among Cancer Patients Undergoing Chemotherapy Using BDI and PHQ-9 Questionnaire.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2014/09/005064
Enrollment
20
Registered
2014-09-25
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: null- cancer patients undergoing chemotherapy treatment

Interventions

None listed

Sponsors

JAMIA HAMDARD
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients must have histologically or cytologically confirmed cancer • Patients receiving chemotherapy for the treatment of cancer • Both male and female patients • Patients capable of giving informed consent • Patients willing to participate in the study

Exclusion criteria

Exclusion criteria: • History of major depression • Meet the DSM-IV criteria for a major depressive episode. • Meet criteria for "treatment resistant" depression defined by failure to, respond to, or intolerance of, at least 2 treatments of antidepressants • Active suicidal ideation • History of any major operation in past 6 months excluding surgeries related to cancer treatment • History of any significant cognitive impairment in past • On any psychotropic medications • Presence of any other concurrent illness(Parkinson disorder; Vascular disorders like Hypertension, Stroke; Endocrine disorders like Type II Diabetes Mellitus, Hypothyroidism; AIDS/HIV and rheumatoid arthritis) • Using any concurrent medication like clonidine, methyldopa, isotretinoin, phenobarbital, levetiracetam, phenytoin, triptans and hormonal agents (corticosteroids, oral contraceptives, GnRH agonists and tamoxifen) or whose side effect is depression • Suffered anxiety episodes in past • History of Schizophrenia • Alcoholics • Habit of any substance of abuse • History of significant dementia or intellectual disability • Incompetent for interview • Psychological, familial, sociological, or geographical conditions that do not permit treatment or medical follow-up and / or prohibit compliance with the study protocol

Design outcomes

Primary

MeasureTime frame
prevalence of depression among cancer patientsTimepoint: patients will be assessed initially at the baseline and the consecutively up to two cycles of chemotherapy

Secondary

MeasureTime frame
to evaluate the incidence of depression according to age,gender, education, stage of cancer,type of cancer, types of chemotherapeutic regiments and cycles of chemotherapyTimepoint: baseline and then up to three cycles of chemotherapy

Countries

India

Contacts

Public ContactDr Nidhi

JAMIA HAMDARD

ilanarang@yahoo.co.in8860624818

Outcome results

None listed

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