Magnetotherapy in Rheumatoid Arthritis Treatment

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

62 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-05-20

Study Completion Date

2020-11-30

Brief Summary

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Participants with rheumatoid arthritis with recommendation to physiotherapy.

Created 3 study groups:

1. Only kinesiotherapy
2. Kinesiotherapy with unipolar magnetic field
3. Kinesiotherapy with bipolar magnetic field

Kinesiotherapy with magnetic field give better effects than only kinesiotherapy.

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Detailed Description

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Participants with rheumatoid arthritis with recommendation to physiotherapy. All participants have dysfunction and pain of hand.

Inclusion criteria:

1. II ° and III ° of advancement of radiological changes
2. II ° and III ° of advancement of functional changes
3. Remission, low or moderate RA activity: DAS28
4. Medical order

1. Magnetotherapy and kinesiotherapy
2. Kinesiotherapy
3. Consent to participate in the study
4. Completion of the research program

Exclusion criteria:

1. Additional physiotherapy treatments for the hands
2. Change in type or dose of pharmacotherapy used
3. Taking steroid anti-inflammatory drugs
4. Malaise and side effects in the subject

Outcome Measures:

1. Duration of morning stiffness
2. The degree of severity of morning stiffness
3. Pain intensity assessment (VAS)
4. Test Box \& Blocks
5. Measurement of the palmar surface of the hand
6. Measuring the range of motion in the joints of the hand
7. Measurement of compression force in a cylindrical grip
8. Time to maintain maximum pressure during cylindrical grip
9. Hand volume measurement
10. HAQ-20 test

Intervention:

1. Group 1: Only kinesiotherapy
2. Group 2: Kinesiotherapy with bipolar magnetic field
3. Group 3: Kinesiotherapy with unipolar magnetic field

Assessment:

1. Immediately before start therapy
2. Immediately after therapy (10 treatments in 2 weeks)

Conditions

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Rheumatoid Arthritis Hand Rheumatism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Only kinesiotherapy

Patients have only kinesiotherapy of hand without steroid anti-inflammatory drugs and magnetotherapy.

Group Type ACTIVE_COMPARATOR

Kinesiotherapy with magnetotherapy

Intervention Type OTHER

Individual kinesiotherapy. Parameters of magnetic field: 7 mT, f= 0-50 Hz, type of impulse: unipolar or bipolar, rectangular pulse

Kinesiotherapy with bipolar magnetic field

Patients have kinesiotherapy of hand and bipolar magnetic field. All patients without steroid anti-inflammatory drugs.

Group Type EXPERIMENTAL

Kinesiotherapy with magnetotherapy

Intervention Type OTHER

Individual kinesiotherapy. Parameters of magnetic field: 7 mT, f= 0-50 Hz, type of impulse: unipolar or bipolar, rectangular pulse

Kinesiotherapy with unipolar magnetic field

Patients have kinesiotherapy of hand and unipolar magnetic field. All patients without steroid anti-inflammatory drugs.

Group Type EXPERIMENTAL

Kinesiotherapy with magnetotherapy

Intervention Type OTHER

Individual kinesiotherapy. Parameters of magnetic field: 7 mT, f= 0-50 Hz, type of impulse: unipolar or bipolar, rectangular pulse

Interventions

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Kinesiotherapy with magnetotherapy

Individual kinesiotherapy. Parameters of magnetic field: 7 mT, f= 0-50 Hz, type of impulse: unipolar or bipolar, rectangular pulse

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* II ° and III ° of advancement of radiological changes
* II ° and III ° of advancement of functional changes
* Remission, low or moderate RA activity: DAS28
* Medical order
* Magnetotherapy and kinesiotherapy
* Kinesiotherapy
* Consent to participate in the study
* Completion of the research program

Exclusion Criteria

* Additional physiotherapy treatments for the hands
* Change in type or dose of pharmacotherapy used
* Taking steroid anti-inflammatory drugs
* Malaise and side effects in the subject

Minimum Eligible Age

35 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No