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Feasibility of Aktiv Gegen Sturzangst (AGES) in Assisted Living Facilities

A Cognitive-Behavioral and Exercise Intervention to Reduce Fear of Falling in Older Adults in Assisted Living Facilities: A Pilot Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07787819
Acronym
AGES
Enrollment
19
Registered
2026-08-26
Start date
2022-09-01
Completion date
2022-12-31
Last updated
2026-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fear of Falling

Keywords

Older adults, Assisted living, Cognitive behavioral therapy, Exercise, Fall prevention, Mobility, Gait

Brief summary

Aktiv Gegen Sturzangst (AGES) is a multicomponent group intervention combining cognitive behavioral therapy and structured exercise to address fear of falling in older adults receiving services from assisted living facilities. This single-arm, non-randomized pilot study evaluated the feasibility of implementing AGES in three assisted living facilities in Switzerland and the feasibility of study procedures and outcome measures for a future controlled trial. Nineteen older adults participated in eight weekly group sessions delivered by trained course leaders. Feasibility outcomes included recruitment, retention, course-leader deployment, protocol adherence, completion of clinical outcome measures, and feasibility of contactless LiDAR-based gait assessment.

Detailed description

AGES was developed as an adaptation of multicomponent approaches to fear of falling for use in German-speaking Swiss assisted living facilities. The intervention consisted of eight weekly group sessions of approximately 60 minutes combining cognitive behavioral therapy-based discussion and reflection with structured balance, strength, mobility, and flexibility exercises. Sessions were delivered by trained facility-based course leaders. The pilot primarily assessed the feasibility of recruitment and retention, course-leader training and deployment, intervention delivery, completion of proposed outcome measures, and LiDAR-based gait assessment. Clinical measures included the Falls Efficacy Scale-International (FES-I), World Health Organization-5 Well-Being Index (WHO-5), and Timed Up and Go test (TUG). The study was exploratory and was not designed or powered to establish intervention effectiveness.

Interventions

BEHAVIORALMulticomponent fear of falling intervention

Eight weekly group sessions delivered by trained course leaders. Sessions included cognitive behavioral therapy-based discussion and reflection addressing emotions, automatic thoughts, safety behaviors, assumptions, goal setting, and self-management, combined with structured exercises performed in seated or supported-standing positions where appropriate.

Sponsors

Eric Lenouvel
Lead SponsorOTHER
Age-Stiftung
CollaboratorUNKNOWN
Public Health Switzerland
CollaboratorUNKNOWN

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Masking description

No masking was used. Participants, course leaders, and investigators were aware that all participants received the AGES intervention.

Intervention model description

Single-group, non-randomized pilot study in which all participants received the AGES intervention. No comparator or control group was included.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 65 years or older * Receiving some level of care or services through a participating assisted living facility * Identified by facility staff as potentially experiencing fear of falling or expressing interest in a fall-prevention program * Able to participate safely in group sessions

Exclusion criteria

* Moderate to severe neurocognitive disorder * Unstable psychiatric illness, including an acute depressive episode or substance use disorder * Physical limitations precluding safe participation in group sessions, including blindness, severe frailty, wheelchair dependence, or requirement for full mobility assistance

Design outcomes

Primary

MeasureTime frameDescription
Course-leader deploymentDuring the 8-week intervention periodNumber and proportion of trained course leaders who subsequently delivered an AGES intervention group
Participant retentionBaseline to approximately 8 weeksNumber and proportion of enrolled participants retained through completion of the intervention
Completion of clinical outcome measuresBaseline and approximately 8 weeksNumber and proportion of participants providing paired FES-I, WHO-5 and TUG assessments
Protocol adherenceThrough approximately 8 weeksNumber of delivering course leaders reporting delivery according to the standardized intervention manual without major deviations
Feasibility of LiDAR gait assessmentAt approximately Week 8, toward the end of the 8-week intervention periodProportion of participants in whom LiDAR measurement could be acquired and proportion of acquired measurements yielding usable processed gait data

Secondary

MeasureTime frameDescription
Falls Efficacy Scale-International (FES-I)Baseline and approximately 8 weeksThe Falls Efficacy Scale-International (FES-I) is a 16-item questionnaire assessing concern about falling during physical and social activities. Each item is scored from 1 (not at all concerned) to 4 (very concerned), giving a total score ranging from 16 to 64. Higher scores indicate greater concern about falling and therefore a worse outcome.
World Health Organization-5 Well-Being Index (WHO-5)Baseline and approximately 8 weeksThe World Health Organization-5 Well-Being Index (WHO-5) is a 5-item questionnaire assessing subjective psychological well-being over the previous two weeks. Each item is scored from 0 (at no time) to 5 (all of the time), giving a total raw score ranging from 0 to 25. Higher scores indicate greater psychological well-being and therefore a better outcome.
Timed Up and Go (TUG) TestBaseline and approximately 8 weeksThe Timed Up and Go (TUG) test assesses functional mobility. Participants are timed, in seconds, while standing up from a chair, walking 3 meters, turning, walking back, and sitting down. The outcome is the time required to complete the test. Lower times indicate better functional mobility, whereas higher times indicate worse mobility.

Countries

Switzerland

Contacts

STUDY_DIRECTORStefan Kloeppel, MD

Department of Old Age Psychiatry and Psychotherapy, University Hospital of Psychiatry (UPZ), Bern

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026