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The effect of empowerment program based on BASNEF model on general health and self-efficacy of hemodialysis patients

The effect of empowerment program based on BASNEF model on general health and self-efficacy of hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017022514086N10
Enrollment
70
Registered
2017-05-06
Start date
2017-04-09
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

Hemodialysis. Chronic kidney disease, stage 5

Interventions

Intervention 1: For intervention group patient, BASNEF-based empowerment program is performed by researchers. Intervention method so that Patients in groups (least 8 people and maximum 15 people) in 8
Behavior
Lifestyle
For intervention group patient, BASNEF-based empowerment program is performed by researchers. Intervention method so that Patients in groups (least 8 people and maximum 15 people) in 8 sessions 60 min
Patients in the control group underwent routine cares and educations and them will gave the hemodialysis patients special educational pamphlet.

Sponsors

Kashan University of Medical Sciences, Vice Chancellor of Research & Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Patients treated with chronic hemodialysis according to specialist diagnosis. 2. Willingness to participate in research. 3. Aged 18 to 65 years. 4. A history of well-known mental problems and kidney transplant is not. 5. Known cognitive problems including Alzheimer's disease, stroke, transient ischemic attack and hearing and vision loss to the extent that they cannot read or write; not suffered. 6. Physical and mental ability have to participate in empowerment meetings and be able to talk. 7. The caregiver is an important person for studying person and trust and confidence family and relatives his/her that directly involved in patient care. Exclusion criteria: 1. Dissatisfaction with continuation of cooperation with the study for any reason and at any phase 2. The absence in two or more sessions in the research program. 3. Outbreak debilitating complications of the disease. 4. Studying person died during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
General health. Timepoint: At baseline and a week after the last session implantation in the intervention group and after a month of the start of the study in the control group. Method of measurement: Goldberg's General Health Questionnaire?.;Self-efficacy. Timepoint: At baseline and a week after the last session implantation in the intervention group and after a month of the start of the study in the control group. Method of measurement: Sherer's General Self-Efficacy Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Aghajani

Kashan University of Medical Sciences

aghajani1362@yahoo.com; aghajani_m@kaums.ac.ir+98 31 5554 0021

Outcome results

None listed

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