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The effect of reflexology on post- electroconvulsive thrapy on severity of pain in depressed patients

The effect of reflexology on post- electroconvulsive thrapy on severity of pain in depressed patients referring to educational-treatmant Razi psychiatric center of Urmia in 2018

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161116030926N1
Enrollment
56
Registered
2018-09-08
Start date
2018-09-14
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Severe depression without symptoms of psychosis. Severe depressive episode without psychotic symptoms

Interventions

Intervention 1: Intervention group: After initial heating, the head will press the reflection points of the head and muscles in the hands and feet (mid-thumb and middle finger) using a reflexology sti

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age: 18-65 years old Having one type of depression (based on documentation of the case and psychiatrist's opinion) that requires ECT Patient is not in the acute phase of psychosis Patient with obvious anomalies in the organs Patient has a willing and informed consent to participate in the study Patient with underlying diseases such as diabetes, hypothyroidism, hypoparathyroidism, musculoskeletal disorders Patient at the time of intervention with perceptual impairment and disorder The patient does not have anxiety disorders according to the diagnosis of the psychiatrist The patient has no acute visual problems. (Due to interference with the filling of the numerical scale of pain) Score 3 or higher on the visual scale of pain assessment No previous massage has been performed Drug addiction or drug intake before the study Not using the drug for at least 4 hours before the intervention

Exclusion criteria

Exclusion criteria: The patient does not have the necessary cooperation to receive the intervention Intervention causes illness and delusions in the patient Patient disclaims continuation of the study for any reason The patient is allergic to the touch and the inability to tolerate massage in the area

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: Measure the severity of pain before the intervention and after the intervention. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Ali Ashraf Jodat

Oroumia University of Medical Sciences

jodat20@yahoo.com+98 44 3275 4961

Outcome results

None listed

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