Psychiatric DisordersNCT00184327
Changes Following Inpatient Child-oriented Family Treatment
An observational study of Psychiatric Disorders, run by Norwegian University of Science and Technology at 5 sites in Norway.
Trial summary
Children receiving IFT (intensive family therapy) were assessed for symptom profile and global functioning before admission, 3 months after discharge and 1 year after discharge. Children were assessed by parents, children, their teachers and themselves. Read more about this study
- Who is it for?
- Ages 6 years and older
- Conditions the study is for
- Psychiatric Disorders
- What is being tested?
- Intensive family therapy - inpatient and Diagnostic assessment - child and adolescent psychiatry
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 150 participants
- Where
- 5 sitesNorway
- Study dates
- Jan 2002to Jun 2008
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Family offered inpatient family treatment in child and adolescent psychiatry
Who may be able to join
- Family offered inpatient family treatment in child and adolescent psychiatry.
Who cannot join
- inpatient treatment terminated prematurely
Trial locations and contacts
5 sites in 1 country.
5 sites in 1 country
Norway5 sites
Haukeland University Hospital, Helse Bergen
Bergen
Levanger Hospital
Levanger
Namsos Hospital
Namsos
Norwegian University of Science and Technology (NTNU), Faculty of Medicine, Dept. of Neuroscience, Center for Child and Adolescent Mental Health
Trondheim, N-7089
St.Olav Hospital
Trondheim
About this study
Official title: Change Across Intensive Inpatient Family Treatment in Child and Adolescent Psychiatry. A Multi-site Study of Parents and Children in Inpatient Family Treatment
Children receiving IFT (intensive family therapy) were assessed for symptom profile and global functioning before admission, 3 months after discharge and 1 year after discharge. Children were assessed by parents, children, their teachers and themselves. Parents were assessed by themselves at the same points in time through psychological self-report questionnaires.
The study is intended to explore covariates to change in children as well as in parents during (pre-treatment) the treatment and follow-up periods.
Read the detailed description
IFT is an intensive combinatory family treatment which is child-oriented, and traditionally used in an inpatient family treatment unit in child and adolescent psychiatry.
Measures include ones on bonding (PBI), personality traits (NEO-PI), anxiety and depressive symptoms (HADS), attributional tendencies (PAT) and social desirable responding (BIDR). A subgroup was also assessed before a waiting period (pre-treatment).
- Conditions
- Psychiatric Disorders
- Being tested
- Intensive family therapy - inpatient, Diagnostic assessment - child and adolescent psychiatry
- Keywords
- Severe and longstanding psychiatric symptoms in children
- Medical subject headings
- Mental Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Intensive family therapy - inpatientBehavioural
2-4 weeks (5days) family inpatient assessment and treatment
Diagnostic assessment - child and adolescent psychiatryBehavioural
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Sep 2005 (estimated)
- Study startJan 2002
- Primary completionDec 2006
- Study completionJun 2008
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Psychiatric DisordersStudies of the same condition, open and under way.
- More trials run by Norwegian University of Science and TechnologyThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 150 participants (actual)
Sponsor and investigators
- Lead sponsor
- Norwegian University of Science and Technology
- Sponsor type
- University, hospital or other
- Collaborators
- Haukeland University Hospital, St. Olavs Hospital, Helse Nord-Trøndelag HF, Namsos Hospital
- Responsible party
- Sponsor
- Investigators
- Tormod Rimehaug, Asst. Prof., Principal investigator, Norwegian University of Science and Technology (NTNU), Faculty of Medicine, Dept. of Neuroscience, Center for Child and Adolescent Mental Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00184327
- Sponsor's protocol ID
- Forskpro p03000213
- Status last verified
- Jan 2017
- First submitted
- 13 Sep 2005
- Last updated
- 18 Jan 2017
- Results posted
- No
- Data monitoring committee
- No
Publications
Rimehaug T, Berg-Nielsen TS, Wallander J. Change in self-reported emotional distress and parenting among parents referred to inpatient child psychiatric family treatment. Nord J Psychiatry. 2012 Sep;66(4):260-7. doi: 10.3109/08039488.2011.630752. Epub 2011 Nov 16.
PubMed 22087555
Study at a glance
From the registry record, last updated by the sponsor on 18 Jan 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Change Across Intensive Inpatient Family Treatment in Child and Adolescent Psychiatry. A Multi-site Study of Parents and Children in Inpatient Family Treatment
- ClinicalTrials.gov ID
- NCT00184327
- Acronym / sponsor ID
- Forskpro p03000213
- Conditions
- Psychiatric Disorders
- Keywords
- Severe and longstanding psychiatric symptoms in children
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 150 participants (actual)
- Lead sponsor
- Norwegian University of Science and TechnologyUniversity, hospital or other
- Collaborators
- Haukeland University Hospital, St. Olavs Hospital, Helse Nord-Trøndelag HF, Namsos Hospital
- Study start
- Jan 2002
- Primary completion
- Dec 2006 (actual)
- Study completion
- Jun 2008 (actual)
- First posted
- 16 Sep 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Children receiving IFT (intensive family therapy) were assessed for symptom profile and global functioning before admission, 3 months after discharge and 1 year after discharge. Children were assessed by parents, children, their teachers and themselves. Parents were assessed by themselves at the same points in time through psychological self-report questionnaires.
The study is intended to explore covariates to change in children as well as in parents during (pre-treatment) the treatment and follow-up periods.
Detailed description
IFT is an intensive combinatory family treatment which is child-oriented, and traditionally used in an inpatient family treatment unit in child and adolescent psychiatry.
Measures include ones on bonding (PBI), personality traits (NEO-PI), anxiety and depressive symptoms (HADS), attributional tendencies (PAT) and social desirable responding (BIDR). A subgroup was also assessed before a waiting period (pre-treatment).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 6 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Family offered inpatient family treatment in child and adolescent psychiatry
Key inclusion criteria (1 listed)
- Family offered inpatient family treatment in child and adolescent psychiatry.
Key exclusion criteria (1 listed)
- inpatient treatment terminated prematurely
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Intensive family therapy - inpatient2-4 weeks (5days) family inpatient assessment and treatment | Behavioural | – |
| Diagnostic assessment - child and adolescent psychiatry | Behavioural | – |
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Jan 2017.
- Results publication: PubMed 22087555Rimehaug T, Berg-Nielsen TS, Wallander J. Change in self-reported emotional distress and parenting among parents referred to inpatient child psychiatric family treatment. Nord J Psychiatry. 2012 Sep;66(4):260-7. doi: 10.3109/08039488.2011.630752. Epub 2011 Nov 16.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Tormod Rimehaug, Asst. Prof. principal investigator
Norwegian University of Science and Technology (NTNU), Faculty of Medicine, Dept. of Neuroscience, Center for Child and Adolescent Mental Health
5 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Psychiatric Disorders, run by Norwegian University of Science and Technology at 5 sites in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 18 Jan 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 sites in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00184327, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jan 2017.