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Home workouts may boost muscle power in kidney patients

NCT ID NCT02923063

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether a personalized, home-based exercise program done via video calls could improve muscle function in people with moderate-to-severe chronic kidney disease (CKD) who are not on dialysis. Thirty-two sedentary adults aged 30-75 with CKD took part. They did combined aerobic and resistance exercises three times a week for 12 weeks. The goal was to see if exercise could boost muscle mitochondria and physical performance, potentially revealing new ways to treat muscle wasting in CKD.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Combined aerobic and resistance exercise via videoconferencing
What this could lead to
If successful, this could point toward exercise programs that improve muscle function and quality of life in people with chronic kidney disease.
What could go wrong
This is a small, early-stage study with only 32 participants. Results may not apply to all kidney disease patients, and the exercise program may not be effective for everyone.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

32 people

The number who actually took part.

Started

Jan 2020

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Moderate-severe CKD determined by estimated glomerular filtration rate (eGFR) \<60ml/min per 1.73m2 * No history chronic treatment with dialysis. * Age 30 years old to 75 years * Sedentary defined as self-reporting no more than 1 day per week of regular (structured) endurance exercise (EE) \[e.g., brisk walking, jogging/running, cycling, elliptical, or swimming activity that results in feelings of increased heart rate or rapid breathing (EE), and/or sweating\] or resistance exercise (RE) (resulting in muscular fatigue) lasting no more than 60 minutes in the past year. * Persons bicycling as a mode of transportation to/from work \> 1 day/week etc. are not considered sedentary * Leisure walkers are included unless they meet the heart rate, breathing and sweating criteria noted above * Persons adherent to both 1 day/week of RE and 1 day/week of EE are excluded Exclusion Criteria: * Current or previous transplantation * Current pregnancy (all females of child-bearing potential will have a pregnancy test) * Wheelchair dependence or other disability that precludes physical exercise * Oxygen dependent Chronic obstructive pulmonary disease (COPD) * Shortness of breath after walking \<100 steps on flat surface * Weight \>300 pounds * HIV infection or hepatitis viral infection * Decompensated cirrhosis * Active malignant cancer other than non-melanomatous skin cancer * Drugs that alter mitochondrial function: * muscle relaxants (methocarbamol, baclofen, tizanidine, carisoprodol, cyclobenzaprine) * oral steroids (Equivalent of 10mg or more of prednisone daily) * anti-viral medications (tenofovir, zalcitabine, didanosine, stavudine, lamivudine, zidovudine, abacavir, adefovir, interferon, ribavirin, efavirenz, dasabuvir, ombitasvir) * oral calcineurin inhibitors (Tacrolimus, Cyclosporine) * Antiepileptic drugs (Phenytoin, phenobarbital, carbamazepine, valproic acid, oxcarbazepine, ethosuximide, zonisamide, topiramate, and vigabatrin) * Antipsychotics (haloperidol, thioridazine, risperidone, quetiapine, clozapine, olanzapine and aripiprazole) * Drugs- anticoagulants or antiplatelets * Anticoagulants, any 1 (coumadin, rivaroxaban, apixaban, dabigatran, edoxaban) * Antiplatelets, any 2 (aspirin, cilostazol, clopidogrel, dipyridamole, prasugrel, ticagrelor, ticlopidine, vorapaxar) * Implants that prohibit MRI measurements or trauma involving metal fragments * Pacemaker * History of clotting disorder (Deep venous thrombosis, pulmonary embolism) or bleeding disorder. * History of sever heart disease/disorders: coronary artery bypass graft (CABG) surgery, atrial fibrillation * Vascular stent: bare metal or any recently placed (within 6 months) * Current substance abuse * Institutionalization * Current participation in an interventional trial * Inability to provide informed consent without a proxy respondent * Non-English speaking * Any condition which in the judgement of the clinical investigator places the participant at risk from participation in the study. Additional Criteria: * On chronic dialysis * Expectation to start dialysis within 6 months. * High dose antioxidants (Vitamine C, Vitamin E) * Baseline systolic blood pressure \>170 or diastolic blood pressure \>100 * Uncontrolled diabetes with a HgbA1c \>8.5 * Active uncontrolled thyroid disease * Anemia (Hgb \<9 g/dL) * Current substance abuse (i.e. amphetamine abuse) * Chronic opioid use (i.e. for chronic pain) * Chronic use of immunosuppressants * Active coronary ischemia detected by ECG on cycle ergometry VO2max testing. These individuals will be promptly referred to their primary care provider by the PI.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • UC Davis Health

    Sacramento, California, 98104, United States