Clinical trial registry record

Effects of Simultaneous Balance and Resistance Training in Older Adults

A registered study indexed because it matched monitored longevity research terms. Registry status: Completed. 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 Completed.
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 September 21, 2015.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT02555033
Last registry update
September 21, 2015
Status
Completed
Phase
Phase not reported
Sponsor
University of Kassel
Enrollment
75
Countries
Germany
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

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

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · NONE
Evidence population
Human clinical study registration
Participants
75
Population
ALL · 65 Years to 80 Years
Duration
2014-02-01 to 2014-09-01
Intervention
Resistance training; Instability resistance training
Comparator
Not reported
Outcomes measured
Maximal isometric leg extension strength (ILES) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days aft…; Fall self-efficacy Questionnaire — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the interven…; Dynamic Balance (stride velocity) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the interve…; Dynamic Balance (stride length & step width) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after…; Dynamic Balance (double support) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the interven…; Proactivec Balance (timed up and go test) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the…; Proactivec Balance (functional reach test) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after th…; Reactive balance (push and release) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the inter…; Power tests (chair rise test) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the interventio…; Power tests (stair power test) — Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the interventi…
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.

  • Resistance training · 100%Title contains controlled term: resistance training. Abstract contains controlled term: resistance training. Source terminology contains: resistance training. Title supplies longevity context: older adult. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 35%. These figures help sort records; they are not medical ratings.

resistance training
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