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Effect of Psychosocial Treatment by the Case Manager in Patients After a Suicide Attempt

Effect of Proactive Psychosocial Treatment by the Case Manager in Patients After a Suicide Attempt: a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00664872
Enrollment
147
Registered
2008-04-23
Start date
2007-08-31
Completion date
2008-07-31
Last updated
2014-01-09

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

Conditions

Suicide, Attempted

Keywords

case manager, suicide, attempt, effectiveness

Brief summary

The purpose of this study is to determine the case manager are effective in the treatment of suicide attempters.

Detailed description

Compared with usual care, interventional group will (1) improve treatment attendance, (2) have less repeated suicide attempts in adults after a suicide attempts, and (3)have better patients' satisfaction with care.

Interventions

OTHERproactive psychosocial intervention by care managers

A case manager will be assigned to each of the participants in the intervention group. All case managers are psychologists. After discharge from the emergency department, the participants receive six sessions of proactive psychosocial intervention by their case manager over four months. Duration of each session is approximately 30 minutes. The intervention consists of telephone or face-to-face contacts with the case manager at scheduled intervals or when clinically necessary. If a patient declines medication therapy from the psychiatrist, case manager will provide psychotherapy using the model of cognitive-behavioural approach and problem-solving therapy. Case managers will receive backup and supervision by psychiatrist investigators and monthly supervision of therapy. Case managers will regularly monitor suicide risk, clinical status and provide follow-up.

BEHAVIORALcase management

Sponsors

National Science and Technology Council, Taiwan
CollaboratorOTHER_GOV
Shen-Ing,Liu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants recruit adults who: 1. Discharge from an emergency department of a teaching hospital after attempt suicide 2. Aged above 18 years old 3. Agree to provide written inform consent.

Exclusion criteria

1. Patients were too ill to be interviewed 2. Patients have immediate and severe suicide risk.

Design outcomes

Primary

MeasureTime frame
treatment adherence, defined as outpatient mental health clinic attendance6-month, and 12-month

Secondary

MeasureTime frame
During follow-up periods (6-month, and 12-month), interventional group will have (1) less repeated suicide attempts (behavior) (2) less suicidal ideation, (3) lower depression score, (4) better patients' satisfaction with care6-month, and 12-month

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026