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The effect of religious/spiritual psychotherapy on the Physical and Psychological health among women patients with breast cancer

The effect of religious/spiritual psychotherapy on improvement of illness perception, inner strength promotion and serum level of CA15-3 among women patients with breast cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016090529715N1
Enrollment
45
Registered
2017-08-11
Start date
2016-09-22
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: Breast cancer. Condition 2: Depression. Condition 3: anxiety. Malignant neoplasm of breast Depressive episode Other anxiety disorders

Interventions

Lifestyle
Intervention 1: intervention group: undergoes ten 90-minute sessions of individual spiritual-religious psychotherapy including God consciousness, prayer, endeavor, kindness and forgiveness, hope, Isl
intervention group: undergoes ten 90-minute sessions of individual spiritual-religious psychotherapy including God consciousness, prayer, endeavor, kindness and forgiveness, hope, Islamic meaning and
placebo group: undergoes a few neutral individual consultation sessions
Control group: routine care

Sponsors

Vice Chancellor for Research and Technology of Semnan University
Lead Sponsor
researcher
Collaborator

Eligibility

Sex/Gender
Female
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: female; pathology report of malignant neoplasm of breast; breast surgery; Completion of chemotherapy and radiation therapy; Having informed consent exclusion criteria: age under 25 or over 60; Metastatic disease; Having serious or chronic medical conditions

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Illness perception. Timepoint: Before intervention, Immediately after the end of the intervention, and Four months after the end of the intervention in the follow-up period. Method of measurement: illness perception questionnaire.;Inner strength. Timepoint: Before intervention, Immediately after the end of the intervention, and Four months after the end of the intervention in the follow-up period. Method of measurement: inner strength questionnaire.;Serum level of CA 15-3 tumor marker. Timepoint: Before intervention, Immediately after the end of the intervention, and Four months after the end of the intervention in the follow-up period. Method of measurement: blood test.

Secondary

MeasureTime frame
Anxiety and depression. Timepoint: Before intervention, Immediately after the end of the intervention, and Four months after the end of the intervention in the follow-up period. Method of measurement: dss questionnaire.;Spiritual health. Timepoint: Before intervention, Immediately after the end of the intervention, and Four months after the end of the intervention in the follow-up period. Method of measurement: spiritual health questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSafoora Davari

Semnan University

sdavari@semnan.ac.ir; davarisafoora51@yahoo.com+98 23 3362 4250

Outcome results

None listed

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