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Pulsed Electromagnetic Fields in Preventing Physical Deconditioning in Patients Undergoing Prolonged Hospitalization

Pulsed Electromagnetic Fields in Preventing Physical Deconditioning in Patients Undergoing Prolonged Hospitalization: A Case Match Control Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06744764
Acronym
PEMF
Enrollment
76
Registered
2024-12-20
Start date
2023-04-17
Completion date
2025-12-31
Last updated
2025-01-08

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

Conditions

Haematological Cancer, Healthy

Keywords

Magnetic therapy, Cancer management, Muscle atrophy

Brief summary

The goal of this clinical trial is to examine if pulsed electromagnetic fields (PEMF) can prevent or decrease physical deconditioning associated with prolonged hospitalisation and immobility of haematology patients. The main question\[s\] it aims to answer \[is/are\]: * Does haematology patients undergoing prolonged hospitalisation have no or decreased physical deconditioning when exposed to PEMF? * What are the changes in muscle secretome at baseline and after exposure to PEMF? Researchers will compare haematology patients who receive PEMF against patients who did not receive the treatment to see if there is a change in physical deconditioning. Healthy volunteers will also be recruited and randomized to either exposure to PEMF or no exposure. Haematology patients will * Have their blood taken at baseline, 4 weeks from baseline and 8 weeks from baseline. * Undergo SPPB test at baseline, 4 weeks and 8 weeks from baseline, and the test comprises of the time up and go test, 4 minute walk test and sit to stand test. * Either expose to PEMF twice per week for 4 consecutive weeks or no exposure. Healthy volunteers will * Have their blood taken at baseline, 4 weeks from baseline and 8 weeks from baseline. * Either expose to PEMF twice per week for 4 consecutive weeks or no exposure.

Interventions

DEVICEPEMF (1mT)

1mT of field strength will be given to patients/healthy volunteers for 10 minutes, twice per week for 4 consecutive weeks.

DEVICEPEMF (0mT)

Healthy volunteers will place their legs in the PEMF device, twice per week for 4 consecutive weeks. However, no magnetic stimulation will be given.

Sponsors

National University Hospital, Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Masking description

Clinical trial coordinators

Eligibility

Sex/Gender
ALL
Age
25 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* Haematology patients who are undergoing induction chemotherapy for acute leukemia * Haematology patients who are undergoing haematopoietic stem cell transplant * Have ECOG 0-24. Able to walk at baseline to participate in short physical battery test. * For healthy volunteers, subjects have to be healthy without any major disease states, not on any drugs or requiring long term medical attention.

Exclusion criteria

* Patients who do not agree to sign the consent form. * Pregnant women will be excluded from the study for healthy volunteers

Design outcomes

Primary

MeasureTime frameDescription
Change in physical deconditioning in haematology patients after 8 sessions of PEMFChange in SPPB test result 4 and 8 weeks from baselineThe haematology patients will undergo the SPPB test which comprises of the time up and go (TUG) test, 4 minute walk test and 5 times sit to stand (STS) test. The same test will be repeated 4 and 8 weeks from baseline. Based on the case study report done previously, we anticipate an improvement of TUG mean by 1.9sec, 5-times STS by 2.3sec and 4 min walk test by 0.14meters by the end of the 8 week therapy. We will consider the trend to be significant if 2 out of 3 three parameters in the SPPB are met.
Changes in the levels of anti-cancer factors in blood plasma from haematology patients and healthy volunteersChange in anti-cancer biomarkers levels in blood plasma from PEMF-exposed patients at week 4 and week 8 versus their own baseline.Anti-cancer factors such as HTRA1 and Klotho can be altered with PEMF therapy in humans.

Countries

Singapore

Contacts

Primary ContactMelissa Ooi, MB BCh, BAO, MRCP(I), FRCPath,
melissa_ooi@nuhs.edu.sg6772 2526

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026