CAlming Touch for People With Agitation or Other Behavioural Symptoms of DEMentia - A Randomized Feasibility Trial

Dementia Clinical Trial

— CADEM  

Official title:

CAlming Touch for People With Agitation or Other Behavioural Symptoms of DEMentia - A Randomized Feasibility Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05272501
• Other study ID #: 200576
• Status: Completed
• Phase: N/A
• Start date: October 4, 2021
• Est. completion date: December 22, 2022

Study information

• Verified date: September 2023
• Source: University College Copenhagen
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Dementia is an increasing health challenge among elderly citizens in Denmark. An estimated 87,000 Danes live with dementia, and this number is expected to increase to 130,000 in 2030. Psychiatric symptoms and behavioral changes decrease quality of life for patients and their spouses and is a challenge for caretakers. Behavior changes include agitation which can be divided in four sub-groups: 1) physical aggression, 2) physical non-aggression, 3) verbal aggression, and 4) verbal non-aggression. Pharmaceutical management of behavioral changes is common and may be associated with negative side-effects including drowsiness and falls. Though non-pharmaceutical interventions such as music, massage and social activities have been recommended the underlying evidence is limited. In this randomized feasibility trial, we will investigate the feasibility and acceptability of therapeutic touch aiming to reduce agitated behavior in people living with dementia in a nursing home that specializes in the care of people living with severe dementia.

The success criteria of this randomized feasibility trial are as follows:

1. Nursing home residents can be recruited and accept the treatment 'CAlming Touch for People with Agitation or Other Behavioral Symptoms of DEMentia' (CADEM) and complete the feasibility project's test protocol.

2. The treatment concept, which involves the nursing staff in charge of the follow-up treatment, can be implemented in practice.

3. The treatment (CADEM) shows a tendency towards less restless and aggressive behavior for demented citizens evaluated based on a validated measuring tool.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: December 22, 2022
• Est. primary completion date: December 22, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Citizens who are residents of the care center due to dementia

• Citizens living at a care center in Naestved Municipality

• Demented citizens who exhibit agitated / aggressive behavior (nursing staff observe whether the citizen exhibits agitated behavior within at least one of the subgroups

Exclusion Criteria:

• Citizens in palliative care

• Citizens who have received BBAUM treatment within the last month

Related Conditions & MeSH terms

• Agitation,Psychomotor
• Behavioral Symptoms
• Dementia
• Psychomotor Agitation

Intervention

Behavioral:
• Calming Touch
The calming treatment consists of deep pressure massage and gentle facilitation. The therapist works with the vertical axis, center, respiration, body boundaries and the feet.

Locations

Country	Name	City	State
Denmark	Distrikt Oest.	Naestved

Sponsors (2)

Lead Sponsor	Collaborator
University College Copenhagen	TrygFonden, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Cohen-Mansfield Agitation Inventory (CMAI) from baseline to 4, 8, and 12 weeks after baseline.	The Cohen-Mansfield Agitation Inventory (CMAI; Cohen-Mansfield, 1986) is a 29-item questionnaire designed to measure the types and frequencies of agitated behaviors exhibited by elderly nursing home residents	CMAI will be performed 2 weeks before baseline, at baseline, and 4, 8, and 12 weeks post baseline.
Secondary	The Erlangen Test for Activities of Daily Living (E-ADL-Test)	The Erlangen Test of Activities of Daily Living (E-ADL-Test) consists of five items: pouring a drink, cutting a piece of bread, opening a small cupboard, washing hands and tying a bow. Each test item underwent standardized evaluation on a scale of 0 to 6.	The E-ADL-Test will be performed at baseline, and 4, 8, and 12 weeks post baseline.
Secondary	Hair cortisol levels	Hair samples will be collected and cortisol levels will be analyzed	Hair samples will be collected at baseline, and 4, 8, and 12 weeks post baseline.