Comparing the effectiveness of schema therapy and psychodrama therapy on body image, social isolation, self-esteem, and phantom pain in mastectomy patients in Tehran.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20251128068136N1

Enrollment

Registered

2025-12-25

Start date

2025-12-30

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Comparing the effectiveness of schema therapy and psychodramatic therapy on body image, social isolation, self-esteem, and phantom pain in mastectomy patients in Tehran..

Interventions

Intervention 1: ntervention group: The first intervention group: 1- A pre-test will be given to the intervention group. 2- The second stage will be given to the first intervention group in 20 90-minut

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Recovering from a mastectomy Lack of definitive diagnosis of comorbid mental disorder Not having any other physical illness or disease other than breast cancer. Informed consent to participate in research

Exclusion criteria

Exclusion criteria: Experiencing a definite diagnosed mental or physical illness during the research An incident or event that has a significant psychological impact on the subject Subject's willingness to abandon treatment

Design outcomes

Primary

Measure	Time frame
The score that the subject will obtain from the Multidimensional Body-Self Relationships Questionnaire will be the body image variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Multidimensional Body-Self Relationships Questionnaire (MBSRQ).;The score that the subject will obtain from the Chalabi and Amirkafi Social Isolation Questionnaire will be the social isolation variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Chalpi and Amirkafi Social Isolation QuestionnaireChalpi and Amirkafi Social Isolation Questionnaire.;The score that the subject will obtain from the Eysenck Self-Esteem Scale will be the self-esteem variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Eysenck Self-Esteem Scale (ESI).;The score that the subject will obtain from the Wang Bakker pain scale will be the phantom pain variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Vankbacker pain scale.	—

Measure

Time frame

The score that the subject will obtain from the Multidimensional Body-Self Relationships Questionnaire will be the body image variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Multidimensional Body-Self Relationships Questionnaire (MBSRQ).;The score that the subject will obtain from the Chalabi and Amirkafi Social Isolation Questionnaire will be the social isolation variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Chalpi and Amirkafi Social Isolation QuestionnaireChalpi and Amirkafi Social Isolation Questionnaire.;The score that the subject will obtain from the Eysenck Self-Esteem Scale will be the self-esteem variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Eysenck Self-Esteem Scale (ESI).;The score that the subject will obtain from the Wang Bakker pain scale will be the phantom pain variable. Timepoint: Pre-test 7 days, post-test 7 days, intervention 60 days, follow-up 60 days after the post-test. Method of measurement: Vankbacker pain scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMona Shukri Shams

Islamic Azad University

shokri@yahoo.com+98 61 3379 8699

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026