Effect of Community Re-entry Program(CRP) on Chronic Mental Illnesses

Evaluation of the effect of community Re-entry Program(CRP) on mental state and social function in chronic psychiatric patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016051424468N2

Enrollment

Registered

2016-05-30

Start date

2015-04-07

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

Chronic Mental Disorder. Bipolar affective disorder,Manic episode, Depressive episode, Schizophrenia

Interventions

Intervention 1: Intervention Group: Community Re-entry Program,16 sessions, two 60-minute to 90-minute sessions per week. Intervention 2: Control group: Did not received Community Re-entry program.

Rehabilitation

Intervention Group: Community Re-entry Program,16 sessions, two 60-minute to 90-minute sessions per week

Control group: Did not received Community Re-entry program

Eligibility

Sex/Gender

All

Age

20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : 1- diagnostic Confirmation of chronic psychiatric disorders by a psychiatrist according to the DSM-IV diagnostic criteria; 2- Aged between 20 and 65 years; 3- At least 2 years passed from the onset of the illness and being in the chronic phase of the disease without a history of symptoms' recurrence , psychotic attack, hospitalization and medical regimen change within last 2 weeks; 4-having the desire to participate in the research and cooperate in all phases of evaluations. Exclusion criteria: 1- Extrapyramidal system disorders (tremor, balance disorders, acute and delayed dystonia, Parkinsonism syndrome) so that social activity is prevented; 2- deafness, blindness and sensation disability that can not be compensated with assistant devices; 3- history of any neurological illness and injuries (such as head trauma, coma, Alzheimer's disease, any type of dementia, epilepsy or stroke); 4-Mental retardation; 5- Electroconvulsive therapy (ECT) in the last 6 months; 6- lack of desire to continue the trial

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Social function. Timepoint: Before and one week after intervention. Method of measurement: Assessment Of communication And Interaction Skill (ACIS) questionnaire.;Mental state. Timepoint: Before and one week after intervention. Method of measurement: Positive And Negative Syndrome Scale(PANSS).	—

Secondary

Measure	Time frame
-. Timepoint: -. Method of measurement: -.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarkhondeh Jamshidi

Hamadan University of Medical Sciences

farkhondeh.jamshidi@yahoo.com+98 81 3838 1571

Outcome results

None listed

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