Strength Training Effects on Musculoskeletal Health

NCT ID: NCT04810975

Last Updated: 2024-08-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-12-02

Study Completion Date

2027-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The objective here is to assess the efficacy of variable resistance muscle training on bone, sleep parameters and quality of life in healthy populations of men and women age 30 or older.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Musculoskeletal Diseases

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

The effect of exercise A on musculoskeletal health

Group Type OTHER

Muscle Strength Training

Intervention Type DEVICE

Strength training occurring specific exercise regimens using Exercise Equipment A or B

The effect of exercise B on musculoskeletal health

Group Type OTHER

Muscle Strength Training

Intervention Type DEVICE

Strength training occurring specific exercise regimens using Exercise Equipment A or B

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Muscle Strength Training

Strength training occurring specific exercise regimens using Exercise Equipment A or B

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 30 years or older (males or females)
* Baseline strength (e.g., can lift an office chair with no problems)
* Be willing to participate in a 6-month RCT
* Be willing to conduct daily muscle training exercises
* Be willing to maintain a food diary
* Be willing to consume \~2.2g/kg body weight daily
* Be willing to submit specimens and conduct tests 3 times over 6 months (0, 3 and 6 months)

Exclusion Criteria

* those who consume vegan or vegetarian diets
* people with conditions like hypertension and uncontrolled non-medicated blood pressure; cardiovascular disease/heart failure (e.g., arrhythmias, unstable angina, congestive heart failure)
* COPD
* drugs that may increase fall risk or make dizzy (e.g., antidepressants, anti-seizure drugs)
* muscle disease (e.g., myasthenia gravis, myopathy, myositis)
* active hernia
* pregnancy
* muscle atrophy (e.g., Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), ALS)
* neuro degenerative disease
* limited mobility
* those who consume proteins supplements.
* Individuals who have implanted pacemakers or defibrillators
* People who suffer from: Marfan syndrome, migraine, hyperparathyroidism, metastatic bone disease, multiple myeloma
* chronic steroid use
* individuals with restrictions to movement and exercise
Minimum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Jaquish Biomedical

INDUSTRY

Sponsor Role collaborator

Duquesne University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Paula Witt-Enderby, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Duquesne University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Duquesne University

Pittsburgh, Pennsylvania, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2020-12-15

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.