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The effect of general and spiritual reminiscence on general health and self-esteem of the elderly residents

The effect of general and spiritual reminiscence on general health and self-esteem of the elderly residents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016043014463N8
Enrollment
64
Registered
2016-05-21
Start date
2016-04-03
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

Mental and behavioural disorders. Reaction to severe stress, and adjustment disorders

Interventions

Intervention 1: Intervention Group: will have typical and spiritual reminiscence program for eight sessions (2 sessions at weeks for 4 weeks). Intervention 2: Control group: Ordinary conversation.
Behavior
Intervention Group: will have typical and spiritual reminiscence program for eight sessions (2 sessions at weeks for 4 weeks)

Sponsors

Vice chancellor for research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
51 Years to 41 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Interested in participating in the study; Able to express their Memories and experiences; Having a support system; Hearing and no blindness; Not receiving any treatment that interfere in mental ability, memory or thinking; Stay in a nursing home for at least 6 months; To have Full consciousness about the time, place and person; Reading and writing literacy; Having the power of writing; Be a resident of the Esfahan city; Be Iranians and Muslim Exclusion criteria: Not wanting to continue the cooperation of the participants during the study; Participate in psychotherapy at the time of the study; Faced with acute stress, such as relatives died during the study; Hospitalization or acute disease; Absence in more than one session; The use of psychiatric drugs affecting public health component (depression, anxiety, sleep, social functioning, effective physical symptoms) during the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
General Health. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: General Health questionnaire.;Self-Esteem. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Rosenberg Self-Esteem Scale.

Secondary

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAyoob Faridi, Zahra Ghazavi

Isfahan University Of Medical Sciences

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

Outcome results

None listed

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