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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01358032
Other study ID # MEC 07-3-064
Secondary ID ZonMw 120610001
Status Completed
Phase N/A
First received May 17, 2011
Last updated July 9, 2012
Start date March 2009
Est. completion date May 2011

Study information

Verified date July 2012
Source Maastricht University Medical Center
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

The main objectives of this study are:

1. an effect evaluation of an in-home multicomponent cognitive behavioural program on concerns about falling and related avoidance of activity (primary outcomes), as well as disability, fall incidents (secondary outcomes) and several additional outcomes in frail community-dwelling older people,

2. a process evaluation of the feasibility of the program, with the following main outcomes: population reached, performance according to protocol, exposure and engagement, opinion on the program of participants and facilitators, perceived benefit or achievement, and experienced barriers and potential solutions, and

3. an economical evaluation on the impact of the program on healthcare utilization and related costs.


Recruitment information / eligibility

Status Completed
Enrollment 389
Est. completion date May 2011
Est. primary completion date May 2011
Accepts healthy volunteers No
Gender Both
Age group 70 Years and older
Eligibility Inclusion Criteria:

- Aged 70 years or over

- At least some concerns about falling

- At least some associated avoidance of activity

- Fair or poor perceived general health

- Living independently in the community

- Written informed consent

Exclusion Criteria:

- Cognitive impairment (a score of less than 4 on the Abbreviated Mental Test 4)

- Language or hearing problems that impede completing an interview by telephone

- Sight problems that impede completing the intervention

- Confinement to bed

- Waiting for nursing home admission

- Permanent use of a wheelchair

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
an in-home cognitive behavioral program
The in-home cognitive behavioral program aims to learn older persons, living in the community, how to deal with concerns about falling and to increase physical, social and functional activity. The principles of cognitive restructuring are used for shifting maladaptive in adaptive attitudes with respect to falling as well as increasing self efficacy beliefs and feelings of control. The following themes are discussed during the program: concerns about falling, thoughts about falling, physical exercise, assert oneself, overcome personal barriers, recognizing fall-ty habits and managing concerns about falling. Duration of the program is 10 weeks with 7 individual sessions (3 home visits (60, 60 and 75 minutes, respectively) & 4 telephone contacts (35 minutes each). The program is facilitated by trained nurses qualified in the field of geriatrics and working for home care agencies.

Locations

Country Name City State
Netherlands Maastricht University Maastricht

Sponsors (2)

Lead Sponsor Collaborator
Maastricht University Medical Center ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

References & Publications (2)

Dorresteijn TA, Rixt Zijlstra GA, Van Eijs YJ, Vlaeyen JW, Kempen GI. Older people's preferences regarding programme formats for managing concerns about falls. Age Ageing. 2012 Jul;41(4):474-81. doi: 10.1093/ageing/afs007. Epub 2012 Feb 23. — View Citation

Dorresteijn TA, Zijlstra GA, Delbaere K, van Rossum E, Vlaeyen JW, Kempen GI. Evaluating an in-home multicomponent cognitive behavioural programme to manage concerns about falls and associated activity avoidance in frail community-dwelling older people: Design of a randomised control trial [NCT01358032]. BMC Health Serv Res. 2011 Sep 20;11:228. doi: 10.1186/1472-6963-11-228. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary concerns about falling Falls Efficacy Scale International (FES-I) baseline, 5 months and 12 months No
Primary avoidance of activities due concerns about falling Falls Efficacy Scale International Avoidance Behaviour (FES-IAB) baseline, 5 months and 12 months No
Secondary disability Groningen Activity Restriction Scale (GARS) baseline, 5 months and 12 months No
Secondary number of falls Fall calendar continuous registration during the course of the trial for a period of 1 year No
Secondary catastrophic beliefs about falling Catastrophic beliefs about falling (CAFS) baseline, 5 months and 12 months No
Secondary perceived consequences of falling CoF - loss of functional independence subscale and damage to identity subscale baseline, 5 months and 12 months No
Secondary perceived control over falling Perceived control over falling (PCOF) baseline, 5 months and 12 months No
Secondary mastery Personal Mastery Scale baseline, 5 months and 12 months No
Secondary feelings of anxiety Subscale of the Hospital Anxiety and Depression Scale (HADS-A) baseline, 5 months and 12 months No
Secondary symptoms of depression Subscale of the Hospital Anxiety and Depression Scale (HADS-D) baseline, 5 months and 12 months No
Secondary social support interactions Social support interactions (SSL 12-I) baseline, 5 months and 12 months No
Secondary health-related quality of life SF-12 Health Survey baseline, 5 months and 12 months No
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