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Performance of ECT Treated Patients on Tactual Performance Test

Performance of ECT Treated Patients on Tactual Performance Test

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2012/06/002755
Enrollment
44
Registered
2012-06-28
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- jor Depressive Disorder (on basis of DSM IV TR)

Interventions

Control Intervention1: Performance of ECT Treated patients on Tactual Performance test compared to Patients on Escitalopram Therapy: No intervention specially for the study would be done and only thos

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Adult male and female subjects who are referred for ECT as well as those who are treated with medication alone. 2 Diagnoses of major depressive Disorder (DSM-IV). 3 Capacity to participate in neuropsychological testing. 4 Preferably, new onset illness in treatment-naive subjects. Or subjects with a Fresh Episode of Depression requiring intervention with antidepressant or ECT 5 Preferably, patients who will likely be available for the 1-month follow up assessment.

Exclusion criteria

Exclusion criteria: 1. Age 2. Mental Retardation 3. Past or Current Neurological Illness (Parkinsons Disease, Epilepsy etc) 4. History of having recieved ECT within past 6 months. 5. Current use of Anti epileptics or Benzodiazepines. 6. Untreated or unstable Medical Condition that may influence Neuropsychological assessments.

Design outcomes

Primary

MeasureTime frame
ECT is associated with greater impairment on the TPT than on a test of verbal (logical) memory. Timepoint: NA

Secondary

MeasureTime frame
Patients receiving ECT perform more poorly on the TPT than those receiving antidepressant drugs Timepoint: NA

Countries

India

Contacts

Public ContactDr Parth Vaishnav

National Institute of Mental Health Sciences

andradec@gmail.com080-2699-5109

Outcome results

None listed

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