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Study of the Validity and Reliability of Two Digital Dynamometers in Older People

Study of the Validity and Reliability of Two Digital Dynamometers in Older People

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06623019
Acronym
SOVARDDIOP
Enrollment
413
Registered
2024-10-02
Start date
2024-12-16
Completion date
2025-04-15
Last updated
2025-12-18

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

Conditions

Frailty, Old Age; Debility, Sarcopenia

Keywords

Muscle Strength Dynamometer, Hand Strength, aged, Muscle Fatigue, Jamar

Brief summary

It is a cross-sectional, randomized, and single-center study with a duration of 6 months. The study will follow the STROBE guidelines for cross-sectional studies and CONSORT 2024. The main objective is to evaluate the validity and reliability of two devices in measuring grip strength and muscle fatigability in community-dwelling older adults.The study will include community-dwelling older adults of both sexes over 60 years of age.

Detailed description

Design: It is a cross-sectional, randomized, and single-center study with a duration of 6 months. The study will follow the STROBE guidelines for cross-sectional studies and CONSORT 2024. The main objective is to evaluate the validity and reliability of the Device 1 and Device 2 devices in measuring grip strength and muscle fatigability in community-dwelling older adults. It will be carried out in two stages: In a first moment the criterion and interobserver validity will be assessed and in a second moment the intraobserver validity. Participants will be randomly assigned to one of the 6 arms to follow different orders of the devices (Device 1, Device 2 or Jamar). Population: community-dwelling older adults of both sexes over 60 years of age. Procedures: The investigators will schedule each participant for the initial assessment day. Using a table of random numbers, they will be assigned one of the arms. All participants have previously read, signed and given their written informed consent. An interview will be conducted in which age, sex and medication will be collected; an anthropometric and functional assessment will be performed. The functional tests include the 30-second squat test and grip strength tests using the Jamar, Device 1 and Device 2. Three repetitions will be performed with each device, allowing 30 seconds between repetitions and 3 to 5 minutes between devices. After 20 minutes the test will be repeated again on the devices for interobserver validation. 5 to 10 days later, tester 1 will repeat the grip test with the same effort to assess intraobserver reliability. Sample size: Similar studies validating grip strength devices compared to the Jamar showed an excellent correlation (ICC \> 0.90). With an estimated ICC of 0.90 ± 0.05 and an alpha risk of 5%, 348 participants are required for the training study. Variables: Sociodemographic (age, sex, hand dominance, number of medication types), anthropometric (height, weight, BMI and SMI), strength and fatigability (total number of repetitions in 30sCS, maximal grip strength (HGS), fatigue resistance (FR) and grip work (GW)) and device preference. Statistical analysis: Maximal strength and fatigability will be analyzed by means of means, standard deviations and statistical tests. Concordance between devices will be assessed using the Kappa coefficient and the Bland-Altman concordance index. ROC curves will be used to determine sensitivity and specificity, and data will be analyzed by gender. Results will be considered statistically significant if p \< 0.05, and IBM SPSS Statistics v28.0 will be used for analysis.

Interventions

DIAGNOSTIC_TESTValidation and reliability

As this is a cross-sectional validation study, there is no intervention.

Sponsors

University of Salamanca
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Community-dwelling older adults of both sexes over 60 years of age.

Exclusion criteria

* Those who do not understand the orders given to them by the researcher or present an obvious advanced state of dementia. * Those people who have amputation in one of the two upper limbs or who cannot perform manual grasping for any reason. * Those who have had an episode of pain in one of the hands during the week prior to the measurement. * Those who, due to any illness, prevent or contraindicate maximum resistance exercises. * Any other cause that the research team assesses that may affect the results.

Design outcomes

Primary

MeasureTime frameDescription
2. Hand grip test2 weeksMeasurement of hand grip strength using a hand-held dynamometer. Values shall be recorded with all three devices.

Secondary

MeasureTime frameDescription
Body Mass Index (BMI)2 weeksIs a mathematical ratio that associates the mass and the size of an individual BMI = weight / height \^2
4. Appendicular Skeletal Muscle mass Index (SMI)2 weeksIs a mathematical ratio that associates the muscle mass and the size of an individual SMI = appendicular muscle mass / height \^2
30 seconds chair stand test (30sCS)2 weeksTest that measures the number of times you perform the maximum number of squats on a chair in 30 seconds. The more squats the better functionally.
Fatigue resistance (FR)2 weeksTime taken to lose 50% of the maximum recorded grip strength.
Grip work (GW)2 weeksValue resulting from multiplying the maximum grip force by the fatigue strength by 0,75. It is measured in watts.

Countries

Spain

Outcome results

None listed

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