Family-centered empowerment model for enhance quality of life of female patients with Pemphigus Vulgaris and active family member.

Not Applicable

• Conditions: Pemphigus Vulgaris.; Pemphigus vulgaris; L10.0

• Registration Number: IRCT2017061934632N1
• Lead Sponsor: Vice chancellor for research, Tarbiat Modares University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 144

Inclusion Criteria

register Pemphigus Vulgaris according to the doctor's diagnosis in the health case
women aged 30-60 years
Patients' and active family member's desire and satisfaction to participate in the research;
Ability to communicate verbally ; provide information and collaborate with the researcher
No mental illness or other acute or chronic illness
Not a member of the health team
having at least literacy to complete the Questionnaire

Exclusion Criteria

the patient and active family member's unwillingness to continue to participate in research
the patient has an acute or chronic illness
the patient has a mental illness
Patient or active family member death

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ifestyle. Timepoint: Before intervention- two months after the end of the intervention. Method of measurement: Walker- Pender health-promoting Lifestyle Questionnaire.

Secondary Outcome Measures

Name	Time	Method
Quality of public life of female patients with Pemphigus Vulgaris and active family member. Timepoint: Before intervention; two months after the end of the intervention. Method of measurement: SF-36 quality of life Questionnaire.;Quality of Exclusive life of female patients with Pemphigus Vulgaris. Timepoint: Before intervention; two months after the end of the intervention. Method of measurement: Iranian version dermatology life quality index (DLQI).;Quality of exclusive life of active family member. Timepoint: Before intervention; two months after the end of the intervention. Method of measurement: The family dermatology life quality index (FDLQI).