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Effectiveness of Mindfulness integrated Cognitive Behavior Therapy in pregnant women

Controlled trial of effectiveness of Mindfulness integrated Cognitive Behavior Therapy on depression, anxiety and quality of life in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015012920869N1
Enrollment
70
Registered
2015-06-02
Start date
2015-02-24
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: Depression. Condition 2: Anxiety. Two or three of the above symptoms are usually present. The patient is usually distressed by these but will probably be able to continue with most activities. Anxiety NOS

Interventions

Mindfulness-integrated cognitive behavior therapy
A systematic therapeutic approach which integrates mindfulness with cognitive behavior therapy. The aim of this approach is to help clients internalize their attention and hence, regulate their emotio
Will receive no intervention.
Behavior
Intervention group
Control group

Sponsors

Vice chancellor for research of Kashan University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria 1. Being in the second to sixth months of pregnancy; 2. Having an age of 18–50 years; and 3. Having a degree in secondary education or higher. Exclusion criteria: 1. Obtaining a score of less than 13 on the Edinburgh Postnatal Depression Scale; 2. Obtaining a score of less than 16 on the Beck Anxiety Inventory; 3. Having a known-cause depression or anxiety following problems such as loss, marital conflicts, unwanted pregnancy, and divorce; 4. Having a history of psychotic disorders; 5. Receiving psychotherapy or drug therapy during past six months; 6. Opting for withdrawing from the study; 7. Failing to participate in more than two sessions of the study intervention; 8. Having a preterm delivery; 9. Having a previous history of suicide; and 10. Having a history of addiction.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: Edinburgh Postpartum Depression Scale.;Anxiety. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: Beck Anxiety Inventory.;Quality of life. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: Quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Yazdanimehr

Kashan University of Medical Sciences and Health Services

rym1368@yahoo.com; yazdanimehr-re@kaums.ac.ir+98 31 5554 0021

Outcome results

None listed

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