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The effect of participation in spiritual groups on quality of life and empowerment in women with breast cancer

The effect of participation in spiritual groups on quality of life and empowerment in women with breast cancer - Shiraz Namazi hospital- 2014.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014050417546N2
Enrollment
74
Registered
2015-04-20
Start date
2014-11-01
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

Breast cancer. Malignant neoplasm of breast

Interventions

Intervention 1: The experimental group will be divided into groups of 5-7 people, the experimental group 5 an hour once a week spiritual sessions will be held in two sessions. If the content of the se
No intervention will conducted for control group.
The experimental group will be divided into groups of 5-7 people, the experimental group 5 an hour once a week spiritual sessions will be held in two sessions. If the content of the sessions will be o

Sponsors

Vice chancellor of research of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. The age range of 18-60 years. 2. The willingness to participate in the study. 3. Having Reading and literacy. 4. Lack of chronic disease and other types of cancer. 5. Lack of mental illness. 6. Breast cancer as the first time and lack of cancer in other breast or any part of body. 7. Left behind the first meeting of chemotherapy and be in second meeting. 8. No evidence of metastatic breast cancer. 9. Lack of intense depression (got score less than 21 from the Beck questionnaire) exclusion criteria :1. The absence of two or more session from spiritual groups. 2. Withdrew from continue to cooperation in participate to research (investigation) in each stage of study. 3. The incidence of unexpected and sever physical or mental injuries.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: before and one month after intervention. Method of measurement: EORTC QLQ-C30 and EORTC QLQ-BR23 Questionnaire.;Empowerment. Timepoint: before and one month after intervention. Method of measurement: The Cancer Empowerment Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Marzieh Momennasab

Hazrate Fatemeh Nursing and Midwifery College

momennasab@sums.ac.ir+98 71 3647 4254

Outcome results

None listed

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