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Clinical Practice Comparison of conflict resolution training and emotional intelligence on the dynamics of families with patients with major depression

Comparison of the combined effect of education on conflict resolution and emotional intelligence training on family resilience of patients suffering from major depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017062234706N1
Enrollment
100
Registered
2017-11-20
Start date
2017-12-21
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

Major depression. Severe depressive episode without psychotic symptoms Recurrent depressive disorder, unspecified Recurrent depressive disorder, current episode severe without psychotic symptoms Severe depressive episode with psychotic symptoms Depressive episode, unspecif

Interventions

Intervention 1: Intervention group: In the first group, conflict resolution training will be provided for two consecutive hours in a two-hourly session per week, according to the protocol. Session 1:
Then he taught and practiced the ways of expressing feelings and desires, teaching and practicing anger management, calming down and answering the questions of the participants. Intervention 2: Interv
Behavior
Intervention group: In the first group, conflict resolution training will be provided for two consecutive hours in a two-hourly session per week, according to the protocol. Session 1: After the group
Intervention group : The session will be taught twice a week for each two hour session. Session 1: Introducing and introducing team members with each other and with the researcher, determining the go
Intervention group: Together, eight sessions of 2 hours will be taught in two sessions. First Session: After the group's acquaintance, about the program's purpose, the importance of the relationship
Control group: In the fourth group, no intervention will be given as a control group

Sponsors

Vice Chancellor of research of Yasouj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criterion: Swirling below 100, having a patient with major depression in the family, written consent for participation in the research, at least 18 years of age, and from each family one male and female, not having mental illness and any other Acute physical illness participant Exclusion criteria: Dissatisfaction with participation in study and death of a patient with major depression?absence in classroom.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Family resilience. Timepoint: Before intervention, after intervention, one month after intervention. Method of measurement: Quicksy's questionnaire.

Secondary

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Khaki

Yasouj? University of Medical Sciences

Sahar khaki136@gmail.ir+98 74 3323 5141

Outcome results

None listed

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