Talking Time: Telephone Support Groups for Informal Caregivers of People With Dementia
Primary Purpose
Caregivers of People With Dementia
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
structured support groups
Sponsored by
About this trial
This is an interventional treatment trial for Caregivers of People With Dementia
Eligibility Criteria
Inclusion Criteria:
- medical ICD-10 dementia diagnosis available for the patient (F00.-*: Alzheimer disease or related disorders, F01.-: Vascular dementia, F03.-:Unspecified dementia)
- living with or sharing cooking facilities with the care recipient or providing care for a relative with diagnosed Alzheimer disease or related disorders for at least 4 hours on at least 4 days of a week for at least the past 6 months, respectively
- access to a telephone connection to be able to participate in the talking Time Intervention and the telephone- based interviews for the evaluation
Exclusion Criteria:
- lack of knowledge of German Language of informal caregiver
- risk of suicide in the informal caregiver
- actual psychiatric diagnosis of mental illness of the caregiver
- ICD-10-diagnosis of Dementia in other diseases classified elsewhere (F02.-*), except Dementia in Primary Parkinson disease (F02.3*) and Lewy Body disease (F02.8/G31.82)
Sites / Locations
- University of Leipzig
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
intervention
control
Arm Description
telephone based structured support groups
Active Comparator: Usual care (intervention as experimental group after 3 month (after T1)
Outcomes
Primary Outcome Measures
Mental Component Summary of the General Health Questionaires Short Form 12 (SF-12)
psychological quality of life of the caregivers
Secondary Outcome Measures
Physical Component Summary of the SF-12
physical quality of life of the caregivers
Perceived Social Support Caregiving Scale
perceived social Support of the caregivers
Caregiver Reaction Scale
caregivers burden
Neuropsychiatric Inventory
neuropsychiatric symptoms of patients
Full Information
NCT ID
NCT02806583
First Posted
June 9, 2016
Last Updated
October 6, 2017
Sponsor
University of Leipzig
Collaborators
German Center for Neurodegenerative Diseases (DZNE)
1. Study Identification
Unique Protocol Identification Number
NCT02806583
Brief Title
Talking Time: Telephone Support Groups for Informal Caregivers of People With Dementia
Official Title
Talking Time: Telephone Support Groups for Informal Caregivers of People With Dementia: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
March 13, 2017 (Actual)
Study Completion Date
May 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Leipzig
Collaborators
German Center for Neurodegenerative Diseases (DZNE)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Caring for people with dementia (PwD) at home requires an enormous amount of time, organization and commitment. Therefore, informal caregivers (ICs), mainly relatives, of PwD often feel a high burden. Even though support groups on-site have shown positive effects on the subjective well-being and on the perceived social support of ICs, relatives either have no time or opportunity to leave the PwD alone or there are no support groups in the vicinity. The Talking Time project therefore aims to close this supply gap by providing structured telephone-based support groups in Germany for the first time. International studies have shown resulting benefits for ICs.
Methods/Design: The project will be evaluated in a cluster adjusted randomized controlled trial. The effects of the 3-months Talking Time intervention will be compared to a normal care group. Outcomes will be measured at two different times (baseline = T0, after 3 months =T1). The control group will receive the Talking Time intervention after T1.
ICs are eligible if they are 18 or older, have cared for the PwD for at least four hours on four days per week in the last six months. Exclusion criteria are psychiatric disorders of the IC.
Primary outcome of the effectiveness elevation is the subjective well-being of the relatives measured by the mental component of the SF-12. Secondary outcomes are the physical component summary of the SF-12, the Perceived Social Support Caregiver Scale, the Caregiver Reaction Scale and the Neuropsychiatric Inventory. For the process evaluation different quantitative and qualitative data sources will be collected addressing reach, fidelity, and dosage.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Caregivers of People With Dementia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
38 (Actual)
8. Arms, Groups, and Interventions
Arm Title
intervention
Arm Type
Experimental
Arm Description
telephone based structured support groups
Arm Title
control
Arm Type
No Intervention
Arm Description
Active Comparator: Usual care (intervention as experimental group after 3 month (after T1)
Intervention Type
Other
Intervention Name(s)
structured support groups
Intervention Description
Telephone-based Support Groups, information booklet and telephone-based preparatory meeting prior to the telephone-based support groups
Primary Outcome Measure Information:
Title
Mental Component Summary of the General Health Questionaires Short Form 12 (SF-12)
Description
psychological quality of life of the caregivers
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Physical Component Summary of the SF-12
Description
physical quality of life of the caregivers
Time Frame
3 months
Title
Perceived Social Support Caregiving Scale
Description
perceived social Support of the caregivers
Time Frame
3 months
Title
Caregiver Reaction Scale
Description
caregivers burden
Time Frame
3 months
Title
Neuropsychiatric Inventory
Description
neuropsychiatric symptoms of patients
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
General Practitioner assessment of COGnition (GPCOG)
Description
cognitive abilities of Patient - Proxy rating
Time Frame
Baseline
Title
Functional Activities Questionnaire
Description
functional activities ability of patients
functional activities ability of patients - proxy rating
Time Frame
3 months
Title
Patient Health Questionaire - 9 items (PHQ-9)
Description
depression of caregivers
Time Frame
Baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
medical ICD-10 dementia diagnosis available for the patient (F00.-*: Alzheimer disease or related disorders, F01.-: Vascular dementia, F03.-:Unspecified dementia)
living with or sharing cooking facilities with the care recipient or providing care for a relative with diagnosed Alzheimer disease or related disorders for at least 4 hours on at least 4 days of a week for at least the past 6 months, respectively
access to a telephone connection to be able to participate in the talking Time Intervention and the telephone- based interviews for the evaluation
Exclusion Criteria:
lack of knowledge of German Language of informal caregiver
risk of suicide in the informal caregiver
actual psychiatric diagnosis of mental illness of the caregiver
ICD-10-diagnosis of Dementia in other diseases classified elsewhere (F02.-*), except Dementia in Primary Parkinson disease (F02.3*) and Lewy Body disease (F02.8/G31.82)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin Berwig, Dr.
Organizational Affiliation
University of Leipzig
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Leipzig
City
Leipzig
State/Province
Saxonia
ZIP/Postal Code
04103
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33417236
Citation
Gonzalez-Fraile E, Ballesteros J, Rueda JR, Santos-Zorrozua B, Sola I, McCleery J. Remotely delivered information, training and support for informal caregivers of people with dementia. Cochrane Database Syst Rev. 2021 Jan 4;1(1):CD006440. doi: 10.1002/14651858.CD006440.pub3.
Results Reference
derived
PubMed Identifier
32838773
Citation
Dichter MN, Albers B, Trutschel D, Strobel AM, Seismann-Petersen S, Wermke K, Halek M, Berwig M. TALKING TIME: A pilot randomized controlled trial investigating social support for informal caregivers via the telephone. BMC Health Serv Res. 2020 Aug 25;20(1):788. doi: 10.1186/s12913-020-05523-9.
Results Reference
derived
PubMed Identifier
28415999
Citation
Berwig M, Dichter MN, Albers B, Wermke K, Trutschel D, Seismann-Petersen S, Halek M. Feasibility and effectiveness of a telephone-based social support intervention for informal caregivers of people with dementia: Study protocol of the TALKING TIME project. BMC Health Serv Res. 2017 Apr 17;17(1):280. doi: 10.1186/s12913-017-2231-2.
Results Reference
derived
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Talking Time: Telephone Support Groups for Informal Caregivers of People With Dementia
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