Clinical Trials Logo

Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03803566
Other study ID # 18-0269
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date August 2025
Est. completion date July 2026

Study information

Verified date November 2021
Source University of Colorado, Boulder
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of the clinical trial is to evaluate the mediating influence of force control on the pegboard times of adults (50-89 years) who are stratified into groups of faster and slower pegboard times. The hypothesis is that practice of either a pegboard test or a force-control task will reduce pegboard times, but the decrease will be greater and less similar after the two practice interventions for the slower group of participants. The outcomes are expected to demonstrate that force control is a modifiable mediator of pegboard times for this cohort, but the effect will be stronger for the group with faster pegboard times.


Description:

The study will involve a randomized, cross-over design with a one-week washout between arms. The two arms (3 weeks each) will comprise practice of the grooved pegboard test and practice of steady contractions while lifting and lowering light loads with a hand muscle. Randomization into practice order will be accomplished with a block approach (block size = 4) for each of the two groups. The outcome assessors will be blinded to practice order. The outcomes will comprise three tests of manual dexterity and the measurement of force control during submaximal contractions. The outcomes will be obtained before and after the six sessions in each practice arm.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2026
Est. primary completion date November 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 89 Years
Eligibility Inclusion Criteria: - Able to read, write, and speak English - Able to arrange transportation to the Boulder campus Exclusion Criteria: - Cognitive impairment - Major psychiatric condition - Unstable depressive disorder - Progressive neurological, muscular, cardiovascular, or skeletal disorder - Chronic pain condition - Currently taking medication known to influence neuromuscular function - Recent hospitalization - Unable to attend 12 practice sessions in 6 weeks

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pegboard practice
Practice of the grooved pegboard test
Force control practice
Practice performing steady muscle contractions

Locations

Country Name City State
United States University of Colorado Boulder Boulder Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Boulder

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Grooved pegboard test Time to complete the test as quickly as possible Changes from baseline (week 1) at weeks 4 and 7
Primary 9-hole pegboard test Time to complete the test as quickly as possible Changes from baseline (week 1) at weeks 4 and 7
Primary Jebsen Hand Function test Time to complete the test as quickly as possible Changes from baseline (week 1) at weeks 4 and 7
Primary Force control The coefficient of variation for force when subjects exert a constant submaximal force Changes from baseline (week 1) at weeks 4 and 7
Secondary EMG amplitude Absolute amplitude of the electromyographic (EMG) signal for the involved muscles during the steady contractions Changes from baseline (week 1) at weeks 4 and 7
Secondary MVC force The peak force exerted during a maximal isometric contractions Changes from baseline (week 1) at weeks 4 and 7
Secondary 1-RM load The maximal weight that can be lifted once Changes from baseline (week 1) at weeks 4 and 7
Secondary Index finger acceleration The average standard deviation of index finger acceleration in the abduction-adduction plane when a light load is being lifted and lowered during the practice intervention Changes from baseline (week 1) at weeks 4 and 7
Secondary Motor unit discharge rates The discharge times of action potentials by motor units during the steady submaximal contractions Changes from baseline (week 1) at weeks 4 and 7
See also
  Status Clinical Trial Phase
Completed NCT05433233 - Effects of Lifestyle Walking on Blood Pressure in Older Adults With Hypertension N/A
Recruiting NCT06032065 - Sequential Multiple Assessment Randomized Trial of Exercise for PAD: SMART Exercise for PAD (SMART PAD) Phase 3
Completed NCT05293730 - Trial of the Impact of the Electronic Frailty Integrated With Social Needs N/A
Recruiting NCT03932162 - Gene Expression Changes In Young and Geriatric Skin Early Phase 1
Completed NCT04064528 - Effects of Age on Amino Acid Delivery to Tendon N/A
Completed NCT03366129 - Blood-Brain Barrier Disruption in People With White Matter Hyperintensities Who Have Had a Stroke
Completed NCT06029920 - Influence of Overground Walking on Biomarkers, Cognitive Function, and Quality of Life in Elderly With Mild Cognitive Impairment N/A
Recruiting NCT05543980 - Leg Heat Therapy in Elderly Individuals Phase 2
Recruiting NCT05566938 - Study to Design a Precision Nutrition Strategy at a Group Level in the Elderly N/A
Completed NCT04894929 - Comprehensive Geriatric Assessment in the Monitoring of Functional Improvement N/A
Not yet recruiting NCT06071130 - Emotion, Aging, and Decision Making N/A
Enrolling by invitation NCT04641663 - Multi-target Dietary Supplement Tolerability in an Aging Population (MTDSST) N/A
Completed NCT04088006 - The Evaluation of Efficacy and Safety of Hyaluronic Acid Injection on Skin Moisturization and Elasticity N/A
Completed NCT03695081 - Patient Pathway Pharmacist - Optimal Drug-related Care N/A
Recruiting NCT05424263 - Acetate and Age-associated Arterial Dysfunction Phase 2
Completed NCT05601713 - Mitigating Heat-induced Physiological Strain and Discomfort in Older Adults Via Lower Limb Immersion and Neck Cooling N/A
Completed NCT04551339 - Zinc Versus Multivitamin Micronutrient Supplementation in the Setting of COVID-19 N/A
Recruiting NCT04997577 - Speech Perception and High Cognitive Demand N/A
Completed NCT05922475 - Efficacy of Pre-sleep or Post-exercise Protein During 12 Weeks of Resistance Exercise Training N/A
Completed NCT04015479 - Peanut Protein Supplementation to Augment Muscle Growth and Improve Markers of Muscle Quality and Health in Older Adults N/A