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Effect of Benson Relaxation method on stress, anxiety and depression in pregnant women

Effect of Benson Relaxation method on stress, anxiety and depression in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201306069463N14
Enrollment
70
Registered
2017-08-16
Start date
2017-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: stress. Condition 2: anxiety. Condition 3: depression. Acute stress reaction Anxiety disorder, unspecified Mild depressive episode

Interventions

Intervention 1: CD of Benson relaxation is gave to case group. after training, case group in one month 2 times daily, morning & evening became relaxed and is assessed in next month & 2 month later w
Behavior
CD of Benson relaxation is gave to case group. after training, case group in one month 2 times daily, morning & evening became relaxed and is assessed in next month & 2 month later with using of DAS
CD of Benson relaxation isn't gave to control group. anxiety, stress and depression is assessed in first visit and in next month & 2 month later with using of DASS-21 questionnaire and compared w

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: INCLUSION criteria:nuli parity, without history of abortion or infertility, women in third trimester of pregnancy, be literacy, ability to use CD of Benson Relaxation and didn't pass similar relaxation course, not using alcohol & opioid, without history of chronic disease, without history of psychologic disorders,without history of using psychoactive drugs, EXCLUSION criteria: without tendency of participants to follow research, pregnancy disorders (e.g: placenta abruption, abnormal presentation and so on), decrease of fetal movement that needs intervention

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: befor & after intervention. Method of measurement: DASS-21 questionnaire.;Stress. Timepoint: befor & after intervention. Method of measurement: DASS-21 questionnaire.;Anxiety. Timepoint: befor & after intervention. Method of measurement: DASS-21 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzade Zenouzi

Tehran University Of Medical Science,Faculty of Nursing & Midvifery

zenozi.az@gmail.com+98 21 3624 8122

Outcome results

None listed

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