Clinical trial registry record

Measuring the Effect of Using the Arabic Otago Exercise Program on Falls and Falls-related Outcomes in Older Adults

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Unknown.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated July 10, 2023.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT05278312
Last registry update
July 10, 2023
Status
Unknown
Phase
Phase not reported
Sponsor
University of Jordan
Enrollment
100
Countries
Jordan
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · SINGLE
Evidence population
Human clinical study registration
Participants
100
Population
ALL · 60 Years
Duration
2022-01-01 to 2023-12-31
Intervention
Otago Exercise Program
Comparator
Control group
Outcomes measured
Incidence of falls — 2 months post intervention.; Incidence of falls — 6 months post intervention.; Incidence of falls — 12 months post intervention.; Fear of Falling (using the Falls Efficacy Scale-International) — 2 months post intervention.; Balance (using Chair balance test and Four test balance scale) — 2 months post intervention.; Mobility (using Timed-Up and go) — 2 months post intervention.; Muscle strength (Hand grip and Quadriceps muscle strength using a dynamometer) — 2 months post intervention.; The Quality of sleep (Using Pittsburgh Sleep Quality Index) — 2 months post intervention.; the severity of Anxiety and Depression (using Hospital Anxiety and Depression Scale) — 2 months post intervention.; The Quality of Life (using Medical Outcomes Study Short Form 12) — 2 months post intervention.; Cognitive ability (using Montreal Cognitive Assessment) — 2 months post intervention.; Sarcopenia (using the bio-impedance analysis) — 2 months post intervention.; Pain (using pain rating scale) — 2 months post intervention.; Activities of daily living (using Katz index of daily living) — 2 months post intervention.
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Exercise · 100%Title contains controlled topic terminology. Summary contains controlled topic terminology. Source terminology contains a controlled topic term. Title supplies ageing or longevity context.

Automated source check 100% · update recency 50%. These figures help sort records; they are not medical ratings.