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The impact of a Body-Centered Protocol and Transcranial Direct Current Stimulation on Enhancing Interoceptive Signal Accuracy in Individuals with Major Depressive Disorder: A double-blind, randomized, sham-controlled clinical trial

The impact of a Body-Centered Protocol and Transcranial Direct Current Stimulation on Enhancing Interoceptive Signal Accuracy in Individuals with Major Depressive Disorder: A double-blind, randomized, sham-controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170417033485N3
Enrollment
40
Registered
2025-10-16
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Depression.

Interventions

Intervention 1: Intervention group: Group 2: No physical therapy but no transcranial electrical stimulation. Intervention 2: Intervention group: Group 3: No physical therapy but transcranial electrica

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Willingness to participate in the therapy sessions Minimum educational attainment of a high school diploma Differential diagnosis of malingering or factitious disorder (confirmed through a diagnostic interview conducted by a psychologist and a psychiatrist) Availability of the patient for at least 6 months to participate in the study and for follow-up discussions Agreement to participate in the research and provision of informed consent Participants must not have been concurrently receiving any other psychological services

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Introceptive signals. Timepoint: The Interoceptive Signals Questionnaire will be administered twice: once as a pre-test before the introduction of the independent variable (treatment), and once as a post-test after the completion of the treatment. Method of measurement: Multidimensional Assessment of Interoceptive Awareness (MAIA).

Secondary

MeasureTime frame
Depression Symptoms. Timepoint: The Beck Depression Inventory (BDI) will be administered before the treatment as a pre-test assessment. Method of measurement: Beck Depression Inventory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza mohamadi

Bagheiat-allah University of Medical Sciences

ar.mohammadi@bmsu.ac.ir+98 912 542 3473

Outcome results

None listed

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