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The effect of life review intervention on depression of elderly male cigarette smokers

The effect of life review intervention on depression of elderly male cigarette smokers: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090304001742N10
Enrollment
36
Registered
2024-03-13
Start date
2024-04-07
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Depression in elderly male smokers. Special screening examination for mental and behavioural disorders

Interventions

Intervention group: In this study, the life review protocol made by Haight and Webster, (1995) will be used. The intervention sessions will be conducted in 6 sessions (one session per week) as follows

Sponsors

Larestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: The samples should have a voluntary desire to participate in the research. Candidates must be at least 60 years old. Candidates should have acceptable hearing and speaking ability. Volunteers should not suffer from cognitive diseases such as dementia. Candidates should not have a history of using psychiatric drugs due to mental problems. Candidates have not received treatment that interferes with mental ability, memory or thinking. Candidates should be familiar with Persian language. Candidates should score 5 to 11 on the elderly depression questionnaire before the intervention. Candidates should have a normal cognitive state (get a score of 25 in the brief examination of mental state). Volunteers should not be present in other treatment groups. Volunteers should have a history of smoking for at least 1 year.

Exclusion criteria

Exclusion criteria: Occurrence of any severe social or family crisis during the study (such as bereavement of family members in the last 6 months) Hospitalization or illness that interferes with conducting the research. Taking nerve pills due to psychological problems during the study. Occurrence of symptoms and signs of crisis when expressing and reviewing life events during the study. Absence from meetings more than once. Alcohol abuse and or drugs. Unwillingness of the samples to continue participating in the research.

Design outcomes

Primary

MeasureTime frame
Scores from 0 to 4 indicate normal, 5 to 8 mild depression, 9 to 11 moderate depression, and 12 to 15 severe depression. Timepoint: Before the intervention, immediately after the intervention. Method of measurement: Elderly Depression Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad-Rafi Bazrafshan

Larestan University of Medical Sciences

mrbazr@sums.ac.ir+98 71 5225 5512

Outcome results

None listed

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