CClinicalTrials.gg
CompletedNCT02985047BASUpdated Aug 28, 2018

Brief Admission Skane: Replacing General Admission for Individuals With Self-harm and Acute Risk of Suicide

An interventional study of Brief Admission in Self-Injurious Behavior, Suicidal Ideation and Suicide, Attempted, sponsored by Region Skane. Completed at 1 site in Sweden. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2018-08-28.

Sponsored by Region Skane · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Sep 2015, registered Nov 2016).
Phase
Not applicable
Study type
Interventional
Enrollment
125
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The purpose of the study is to test a standardized version of brief admission (BA) through randomized controlled trial (RCT). The main objective is to evaluate if BA can serve as a crisis management model for individuals with recurrent self-harm, including suicide attempts and at least three symptoms of Borderline Personality disorder. Participants will be allocated to BA + Treatment as Usual (TAU) or TAU.

Read the detailed description

When individuals with recurrent self-harm and suicidal behaviour seek acute admission to hospital due to a crisis and associated increased suicidal ideation, recommendations for clinical care are still conflicting. The risk for iatrogenic effects of inpatient care are considerable, and long hospital admissions without a clear treatment structure may predict decompensation in functioning. This has resulted in a clinical practice of avoiding admission for individuals diagnosed with Borderline Personality Disorder (BPD).

Brief admission (BA) as an intervention has a longstanding history in the delivery of mental health services in the Netherlands. The core elements of brief admission were determined through consultation with Dutch researchers, interviews with individuals with experience, Dutch clinicians familiar with Brief Admission, and local guidelines from hospitals familiar with implementing this crisis management intervention. Core elements of the intervention were standardized into a protocol, and an educational manual was developed to train clinicians involved in the trial. An objectively rated fidelity measure was developed in order to ensure adherence.

02

Conditions studied

  • Self-Injurious Behavior
  • Suicidal Ideation
  • Suicide, Attempted
  • Borderline Personality Disorder
  • Emergency Services, Psychiatric

Keywords

  • Brief admission
  • admission
  • deliberate self-harm
  • self-harm
03

In context

Emergencies

1,692 studies on the registry are indexed under Emergencies; 333 are open to participants now.

This study's enrollment of 125 is below the median of 145 across 931 interventional studies indexed under Emergencies.

Browse Emergencies studies →

Lead sponsor

Region Skane is the lead sponsor of 372 studies on the registry; 113 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Current episodes of self-harm and/or recurrent suicidality.
  • Fulfilling at least three criteria for borderline personality disorder.
  • Admitted to psychiatric hospital for acute care for at least 7 days or presenting to the psychiatric emergency department at least 3 times during the last six months.

Exclusion criteria

Exclusion Criteria:

  • No regular contact with outpatient psychiatric services.
  • Homelessness. Housing crises are outside the scope of this RCT.
  • Medical disorder from other organs that significantly contributes to inclusion criteria (e.g. if self-harm only occurs during episodes of hypoglycemia in a diabetic patient).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
125 participants (actual)

Study arms

  • Experimental
    Brief Admission

    Participants randomised to Brief admission (BA) will have the possibility of admitting themselves to hospital for a maximum duration of three consecutive days at a maximum frequency of three times per month. Apart from BA they have access to all psychiatric care that they would have if they had not participated in the study (including general admission to hospital).

    Other: Brief Admission

  • No intervention
    Control

    Participants randomized to Treatment as Usual will receive no intervention from the study protocol, except the baseline assessments and repeated assessments administered on the same schedule as described above for the treatment group. They will not be given the evaluation measures that are specific to the intervention. Participants have access to all psychiatric care that they would have if they had not participated in the study (including general admission to hospital).

Interventions

  • OtherBrief Admission

    Participants randomised to Brief admission (BA) will participate in a negotiation together with their out-patient clinician and a representative from the ward. The aim of the negotiation is to form an individualised contract defining how BA will work for them. After signing the contract, will have the possibility to admit themselves to hospital according to the procedure stated in the contract.

    Also known as: Brukarstyrd Inläggning (Swedish)

06

What researchers measure

Primary outcomes

  1. Number of days with hospital admission

    Number of days with Brief admission, general admission, forced (involuntary) admission

    Time frame: Change between the period from 12 month retrospectively to Baseline and the period from baseline to 12 months prospectively

Secondary outcomes

  1. Frequency of forced acts (e.g. restraints and forced medication)

    Time frame: Change between the period from 12 month retrospectively to Baseline and the period from baseline to 12 months prospectively

  2. Individuals' Experiences of the intervention

    Outcome from the questionnaires developed for the method: Individual's Experience Scale (IES)

    Time frame: Data collected at each Brief Admission during a period of 140 weeks. A Brief Admission is defined as a hospital admission according to the procedure defined in the Brief Admission Skane Standardised Protocol.

  3. Clinicians' Experiences of the intervention

    Outcome from the questionnaires developed for the method: Clinician's Experience Scale (CES)

    Time frame: Data collected at each Brief Admission during a period of 140 weeks. A Brief Admission is defined as a hospital admission according to the procedure defined in the Brief Admission Skane Standardised Protocol.

  4. Frequency of all self-harming behaviours including suicide attempts

    Outcome from Five Self-Harm Behaviour Groupings Measure (5S-HM)

    Time frame: Change in frequency between baseline, 6 months and 12 months prospectively.

  5. Severity of self-harming behaviours

    Outcome from Five Self-Harm Behaviour Groupings Measure (5S-HM)

    Time frame: Change in severity between baseline, 6 months and 12 months prospectively.

  6. Level of functioning in activities of daily life

    The World Health Organization Disability Assessment Schedule II (WHODAS 2.0)

    Time frame: Change in ratings between baseline, 6 months and 12 months prospectively.

  7. Ability to cope effectively with life stress

    The Brief COPE

    Time frame: Change in ratings between baseline, 6 months and 12 months prospectively.

  8. Ability to regulate emotions

    The Difficulties in Emotion Regulation Scale

    Time frame: Change in ratings between baseline, 6 months and 12 months prospectively.

  9. Global psychiatric symptoms

    Outcome from Clinical Global Impression Severity Scale

    Time frame: Change in ratings between baseline, 6 months and 12 months prospectively.

  10. Satisfaction with health care

    Client Satisfaction Questionnaire (CSQ)

    Time frame: Change in ratings between baseline, 6 months and 12 months prospectively.

07

Study locations

1 site
  • Division of Psychiatry, Region Skåne
    Lund, Skåne 22185, Sweden
08

References and documents

Publications

  • Witt KG, Hetrick SE, Rajaram G, Hazell P, Taylor Salisbury TL, Townsend E, Hawton K. Psychosocial interventions for self-harm in adults. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013668. doi: 10.1002/14651858.CD013668.pub2. PubMed 33884617 ↗
  • Storebo OJ, Stoffers-Winterling JM, Vollm BA, Kongerslev MT, Mattivi JT, Jorgensen MS, Faltinsen E, Todorovac A, Sales CP, Callesen HE, Lieb K, Simonsen E. Psychological therapies for people with borderline personality disorder. Cochrane Database Syst Rev. 2020 May 4;5(5):CD012955. doi: 10.1002/14651858.CD012955.pub2. PubMed 32368793 ↗
  • Westling S, Daukantaite D, Liljedahl SI, Oh Y, Westrin A, Flyckt L, Helleman M. Effect of Brief Admission to Hospital by Self-referral for Individuals Who Self-harm and Are at Risk of Suicide: A Randomized Clinical Trial. JAMA Netw Open. 2019 Jun 5;2(6):e195463. doi: 10.1001/jamanetworkopen.2019.5463. Erratum In: JAMA Netw Open. 2019 Oct 2;2(10):e1913724. doi: 10.1001/jamanetworkopen.2019.13724. PubMed 31173128 ↗
  • Helleman M, Lundh LG, Liljedahl SI, Daukantaite D, Westling S. Individuals' experiences with brief admission during the implementation of the brief admission skane RCT, a qualitative study. Nord J Psychiatry. 2018 Jul;72(5):380-386. doi: 10.1080/08039488.2018.1467966. Epub 2018 Apr 27. PubMed 29703119 ↗
  • Liljedahl SI, Helleman M, Daukantaite D, Westrin A, Westling S. A standardized crisis management model for self-harming and suicidal individuals with three or more diagnostic criteria of borderline personality disorder: The Brief Admission Skane randomized controlled trial protocol (BASRCT). BMC Psychiatry. 2017 Jun 15;17(1):220. doi: 10.1186/s12888-017-1371-6. PubMed 28619050 ↗

Study documents

  • Protocol and statistical analysis plan · Apr 23, 2018

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 28, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02985047
Lead sponsor
Region Skane
Collaborators
Lund University, Radboud University Medical Center
Responsible party
Sofie Westling (MD, PhD, Region Skane) — Principal investigator
First posted
Dec 7, 2016
Start date
Sep 1, 2015
Primary completion
Jun 30, 2018
Completion
Aug 10, 2018
Last update
Aug 28, 2018

Study contacts

Sofie Westling, MD PhD
principal investigator · Region Skåne

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

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