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positive thinking training on stress, anxiety, depression and quality of life of hemodialysis patients

The effect of positive thinking training on stress, anxiety, depression and quality of life of hemodialysis patients: A randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200514047435N1
Enrollment
70
Registered
2020-05-19
Start date
2020-06-09
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Quality of life, Stress, anxiety and depression of hemodialysis patients. Chronic kidney disease, stage 5

Interventions

Intervention 1: Intervention group: Positive training program was developed based on research and positive intervention programs, as well as internal and external studies in the field of positive educ
at the end of each session, the participants' questions were answered and the next sessions commenced with a review of the topics of the previous session. Multimedia facilities such as computers, vid
also, catering and short breaks were used. One week after the end of the intervention, stress, anxiety, depression, and quality of life questionnaires were filled out by the participants in both group

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: willingness to participate in the study age 18-70 years end-stage renal disease and under hemodialysis a history of hemodialysis for at least 12 months or more lack of participation in other training courses at the same time

Exclusion criteria

Exclusion criteria: history of participate in positive thinking training treatment with psychotropic drugs

Design outcomes

Primary

MeasureTime frame
Stress score based on dass-21 questionnaire. Timepoint: One week after the intervention. Method of measurement: dass-21 questionnaire.;Depression score based on dass-21 questionnaire. Timepoint: One week after the intervention. Method of measurement: dass-21 questionnaire.;Anxiety score based on dass-21 questionnaire. Timepoint: One week after the intervention. Method of measurement: dass-21 questionnaire.;Quality of life based on QOL-sf36 questionnaire. Timepoint: One week after the end of the intervention. Method of measurement: SF-36 Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Sheidaie

Fasa University of Medical Sciences

Sh.amir1390@yahoo.com0098 53333541

Outcome results

None listed

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