DementiaTESAMNCT01217268
Use of Telemedicine in Collaboration Between a Psychogeriatric Unit and Nursing Homes
A study testing Training in person centered care by supervision using video-conference in people with Dementia and Behavioural Disorders, run by Sykehuset Innlandet HF at 1 site in Norway.
Trial summary
The investigators want to evaluate the use of video-conference in the collaboration between the investigators psychogeriatric department and nursing homes. The study aim is to give supervision on a regular basis to the caregivers on a special care unit for patients with dementia with behavioural disturbances during a… Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Dementia, Behavioural Disorders
- What is being tested?
- Training in person centered care by supervision using video-conference
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteNorway
- Study dates
- Oct 2010to Sep 2011
- Phase
- Interventional
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Being resident in a special care unit for persons with dementia
Who cannot join
- Shorter stay than four weeks before inclusion
- terminally ill
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Use of Telemedicine in Collaboration Between a Psychogeriatric Unit and Nursing
The investigators want to evaluate the use of video-conference in the collaboration between the investigators psychogeriatric department and nursing homes. The study aim is to give supervision on a regular basis to the caregivers on a special care unit for patients with dementia with behavioural disturbances during a period of half a year. The investigators want to investigate the impact on caregivers and patients by applying certain tests at baseline, during the intervention and half a year after the intervention.
- Conditions
- Dementia, Behavioural Disorders
- Being tested
- Training in person centered care by supervision using video-conference
- Medical subject headings
- Dementia, Mental Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Training in person centered care by supervision using video-conferenceBehavioural
The investigators will use video-conference for supervising and training of staff members in nursing homes
| Study group | Role | What they receive |
|---|---|---|
| Training and supervision of staff | Experimental | Staff members get training in person centered care by supervision using video-conference kit Receives: Behavioral: Training in person centered care by supervision using video-conference |
What is being measured
The primary outcome is the main question the study is designed to answer.
Neuropsychiatric inventory - nursing home version (NPI-NH)
The investigators want to find out if a supervision of staff members over a six months time, using video-conference technic, contributes to improvement in patients' behaviour registered by NPI-NH
Measured: week 48
Secondary outcomes (1)
Person-centered Care Assessment Tool (P-CAT) Person centered care assessment tool (P-CAT)
Measures the effect of our intervention related to apply person centred dementia care
Measured: week 48
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Oct 2010 (estimated)
- Study startOct 2010
- Primary completionSep 2011 (estimated)
- Study completionSep 2011 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DementiaStudies of the same condition, open and under way.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Sykehuset Innlandet HF
- Sponsor type
- University, hospital or other
- Collaborators
- Norwegian Department of Health and Social Affairs
- Investigators
- Oskar H Sommer, PhD, Principal investigator, SykehusetInnlandet, Norway
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01217268
- Sponsor's protocol ID
- TESAM
- Acronym
- TESAM
- Status last verified
- May 2011
- First submitted
- 22 Sep 2010
- Last updated
- 7 Sep 2018
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 7 Sep 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Use of Telemedicine in Collaboration Between a Psychogeriatric Unit and Nursing
- ClinicalTrials.gov ID
- NCT01217268
- Acronym / sponsor ID
- TESAM / TESAM
- Conditions
- Dementia, Behavioural Disorders
- Study type
- Interventional
- Recruitment status
- Withdrawn
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Sykehuset Innlandet HFUniversity, hospital or other
- Collaborators
- Norwegian Department of Health and Social Affairs
- Study start
- Oct 2010
- Primary completion
- Sep 2011 (estimated)
- Study completion
- Sep 2011 (estimated)
- First posted
- 8 Oct 2010 (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.
The investigators want to evaluate the use of video-conference in the collaboration between the investigators psychogeriatric department and nursing homes. The study aim is to give supervision on a regular basis to the caregivers on a special care unit for patients with dementia with behavioural disturbances during a period of half a year. The investigators want to investigate the impact on caregivers and patients by applying certain tests at baseline, during the intervention and half a year after the intervention.
Study design
- Primary purpose
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Training and supervision of staff | Experimental | Behavioral: Training in person centered care by supervision using video-conferenceStaff members get training in person centered care by supervision using video-conference kit |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Being resident in a special care unit for persons with dementia
Key exclusion criteria (2 listed)
- Shorter stay than four weeks before inclusion
- terminally ill
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 |
|---|---|---|
| Training in person centered care by supervision using video-conferenceThe investigators will use video-conference for supervising and training of staff members in nursing homes | Behavioural | Training and supervision of staff |
Primary outcome
Neuropsychiatric inventory - nursing home version (NPI-NH)
Time frame: week 48
The investigators want to find out if a supervision of staff members over a six months time, using video-conference technic, contributes to improvement in patients' behaviour registered by NPI-NH
1 secondary outcome
Person-centered Care Assessment Tool (P-CAT) Person centered care assessment tool (P-CAT)
Time frame: week 48
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Sep 2018.
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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.
Oskar H Sommer, PhD principal investigator
SykehusetInnlandet, Norway
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Training in person centered care by supervision using video-conference in people with Dementia and Behavioural Disorders, run by Sykehuset Innlandet HF at 1 site 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 2 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: withdrawn, as of the sponsor's last update on 7 Sep 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site 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 was withdrawn before enrolling participants, so there are no results.
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.
What does the primary outcome measure?
Neuropsychiatric inventory - nursing home version (NPI-NH) (time frame: week 48). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 7 Sep 2018.