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Effect of fordyce, s happiness program on stress, anxiety and depression of patients being treated with hemodialysis

Effect of fordyce, s happiness program on stress, anxiety and depression of patients being treated with hemodialysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062914463N5
Enrollment
50
Registered
2015-08-31
Start date
2015-06-05
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: Mental and behavioural disorders. Condition 2: Mental and behavioural disorders. Condition 3: Mental and behavioural disorders. Other anxiety disorders Depressive episode Reaction to severe stress, and adjustment disorders

Interventions

Intervention 1: For study group had Fordyce s happiness program for 6 weeks, one session per week (each session 20 min) by the researcher at the time of hemodialysis. Intervention 2: For other groups
Behavior
For study group had Fordyce s happiness program for 6 weeks, one session per week (each session 20 min) by the researcher at the time of hemodialysis.
For other groups (placebo group) 3 sessions in the form of conversation,keeping in touch and hearing patients problems by colleague researcher individually.

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients age are between 20 to 75; Patients that hemodialyzes due to end stage renal disease; Patients that have active document in hemodialysis centers; Hemodialysis onset 3 months at least; Hemodialysis do with sodium bicarbonate 3 times a week; They should not participate in any complementary treatments during this study; They should not take any drug to control depression, anxiety or stress; They do not have any intellectual or physical disability; Having full consciousness, acceptable reading and writing ability to answer the questions Exclusion criteria:Absent in two continuous fordyce s happiness sessions during study; Patients who giving kidney graft or going under peritoneal dialysis; Patients who do not like to participate in every level of study; Patients start taking drugs to control depression, anxiety and stress in prescribed by physician; Death

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Stress. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: DASS 21 questionnaire.;Anxiety. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: DASS 21 questionnaire.;Depression. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: DASS 21 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYounes Mehrabi koshki, Zahra Ghazavi

Isfahan University Of Medical Sciences

zahra_ghazavi@nm.mui.ac.ir; y.mehrabi@gmail.com+98 31 3792 7580

Outcome results

None listed

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