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IFC Therapy in Proximal Humerus Fractures

Does Interferential Current Provide Additional Benefit to the Rehabilitation Program for the Patients With Proximal Humeral Fractures? A Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04553497
Enrollment
35
Registered
2020-09-17
Start date
2014-04-01
Completion date
2015-10-15
Last updated
2023-11-24

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

Conditions

Interferential Current in Proximal Humerus Fractures

Keywords

Proximal humerus fracture, interferential current, Constant-Murley score

Brief summary

Proximal humerus fractures (PHFs) frequently occur in the elderly and osteoporotic population, but these fractures are also common in individuals under age 60 years. Conservative treatment of PHF usually involves a short period of immobilization followed by orthopedic rehabilitation. However, the severe pain of some patients with fractures limits their participation in the exercise programme, and shoulder muscle atrophy and frozen shoulder may occur in these patients due to immobilization. There are conflicting results regarding the use of physical therapy modalities in the shoulder pain management. Interferential current (IFC) therapy is believed to be effective for the pain-relieving through several mechanisms. Although IFC has been investigated in many painful shoulder disorders, there is no reported study on the effectiveness of IFC therapy in patients with PHF. This study aimed to investigate the effectiveness of IFC added to exercise on shoulder function, pain, and disability compared with placebo in patients with conservative treated PHF. Patients were evaluated within the first week of PHF and divided into two groups to receive either IFC or sham using a simple randomization method. The orthopedic rehabilitation programme was applied to all patients three times a week for four weeks under the guidance of the same physiotherapist. IFC or sham therapy was applied three times a week for 20 minutes before each exercise session by another physiotherapist. Shoulder functions, pain (visual analogue scale), disability and range of motion was evaluated at the end of the rehabilitation program, at 6-weeks and 18-weeks post-treatment by the physiatrist (ED) who did not know which group the patients belonged to. In addition, the amount of acetaminophen usage was noted at each visit.

Detailed description

Patients with conservatively treated proximal humerus fracture who admitted to Ege University Physical Medicine and Rehabilitation outpatient clinic have been included in the study. All patients who met inclusion criteria were enrolled into the study at the first week of PHF. The orthopedic rehabilitation programme was applied to all patients three times a week for four weeks under the guidance of the same physiotherapist. The patients also received a complete set of premade exercise cards, which showed all exercises to ensure that the training program was learned correctly. The patients were recruited at the first week after proximal humerus fracture and then allocated into the groups. The patients were separated into two groups as interferential current or sham using a simple randomization method managed by an impartial observer. Flipping a coin was used for simple randomization (heads - sham, tails - treatment). The patient's group was reported to the physiotherapist who would apply interferential current in a closed envelope. Patients and the outcome assessor were blind to the treatment groups. The IFC therapy was applied using a combined electrotherapy device SONOPULS 692® (brand: Enraf-Nonius). The medium frequency of the IFC was 4000 Hz and 4100 Hz to produce the amplitude-modulated frequency at 100 Hz. Two rubber electrodes (8×6 cm) were fitted on the fractured shoulder. One of the electrodes was placed on the lateral part of the deltoid muscle; the other one was placed on the trapezius muscle near the shoulder. The current intensity was set to achieve a strong but comfortable tingling without visible muscle contraction. The sham therapy consisted of placing the same pads for the same time, but no electrical stimulation was applied to the probes. The primary outcome was shoulder global function which was measured by the Constant-Murley score (CMS). The questionnaire assesses four shoulder functions: 1) pain; 2) activities of daily living (sleeping, work, leisure); 3) range of motion; and 4) muscle strength. The total score ranges from 0 to 100, with a higher score indicating better shoulder function. Activity pain was measured with the visual analog scale (VAS). In addition, in order to evaluate shoulder function and disability, the Disability of the Arm, Shoulder and Hand questionnaire (DASH) was used. This self-administered questionnaire includes 30 questions evaluated on a 5-point Likert scale, most of which relate to the individual's capacity to realize a task. The patients were allowed to use paracetamol during the study and the paracetamol intake was recorded as gr/week. Clinical assessments were evaluated at the end of the treatment, at 6-weeks and 18-weeks post-treatment. Only VAS resting pain was evaluated at the enrollment because the fractured side was immobile when the patients were included in the study. The physician who assessed the treatment outcomes, the patients and the physiotherapist who administer the exercises were unaware of the patient's group of treatment. A clinically meaningful difference was considered to be a change of 15 points in total CMS. In order to detect this improvement, the number of patients needed was 17 per group according to a power of 0.80, a high size effect (d=0.88), a p value of 0.05, and a 15% dropout rate. Statistical analysis was performed using SPSS version 20.0 (IBM, Armonk, NY, USA). An intention-to-treat analysis was employed for all analysis. The variables were investigated using visual (histogram, probability plots) and analytic methods (Kolmogorov-Smirnov, skewness and curtosis) to determine whether they were normally distributed or not. . Continuous data were described as median (inter-quartile range, IQR) or mean (standar deviation, SD) and categorical variables as percentages. Chi-square or Fisher's exact test was used to compare categorical variables and Mann-Whitney U test/Student's T-test was used to compare continuous variables. All outcome values were presented in mean and standard deviation. The repeated measures ANOVA test was used in comparison of the means of the repeated measures. The results of the repeated measures ANOVA were analyzed by Mauchly's sphericity test. If the parametric tests (factorial design for repeated measures analysis) did not provide the preconditions, the Greenhouse-Geisser correction was used for corrections to the degrees of freedom or Friedman's Test. The Bonferroni correction was used for multiple comparisons. A p value of less than 0.05 was considered to show a statistically significant result.

Interventions

Interferential current or sham were applied to the patients before the each exercise session. Pre-modulated bipolar method with the currier frequency of 4 kHz by a combination therapy unit (Sonopuls 692, Enraf-Nonius) with two electrodes (8×6 cm) was used. One electrode was placed on the lateral part of the deltoid muscle; the other was placed on the trapezium muscle close to the shoulder. Subjects were told that in order to produce an effect, the intensity of the stimulator must be maintained at a strong but comfortable level at all times. The sham interferential current therapy consisted of the placement of the same pads for the same time but no electrical stimulation was applied to the probes.

OTHERRehabilitation program

The orthopedic rehabilitation programme was applied to all patients three times a week for 4 weeks under the guidance of the same physiotherapist. The first phase (0-3 weeks) involved the elbow, wrist, and hand active range of motion (ROM) and pendulum (clockwise and counterclockwise) exercises in the 0-2 weeks of the non-displaced fracture. For displaced fractures, elbow, wrist, and hand active range of motion was started immediately, but pendulum exercises were initiated two weeks later. The patients were instructed to continue exercises 3-5 times per day for 30 minutes. After two weeks, active assistive ROM and isometric exercises were performed supine position. During the second phase (3-6 weeks), active forward elevation in supine was carried out and then progressed to sitting and standing position. At the end of the sixth week, a home exercise program was given by the physiotherapist, including resistance exercises using an elastic band (Thera-Band).

Sponsors

Ege University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Patients and the outcome assessor were blind to the treatment groups.

Intervention model description

After the patients were randomized, interferential current was applied for 3 times a week before the each exercise session by another physiotherapist. Pre-modulated bipolar method with the currier frequency of 4 kHz by a combination therapy unit (Sonopuls 692, Enraf-Nonius) with two electrodes (8×6 cm) was used. One electrode was placed on the lateral part of the deltoid muscle; the other was placed on the trapezium muscle close to the shoulder. Subjects were told that in order to produce an effect, the intensity of the stimulator must be maintained at a strong but comfortable level at all times. The sham interferential current therapy consisted of the placement of the same pads for the same time but no electrical stimulation was applied to the probes.

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

were as follows: age ≥ 40 years, PHFs did not require surgery by the orthopedic surgeon, and admission to our outpatient clinic within the first two weeks after the fracture

Exclusion criteria

* Any surgery history for shoulder pathologies * Previous electrotherapy experience before the fracture (to ensure blinding of therapy) * Any contraindication such as pacemaker, malignancy, pregnancy, etc. for IFC * Rheumatic disease such as rheumatoid arthritis and ankylosing spondylitis * Shoulder subluxation; having other fractures in addition to the PHF * Known or suspected joint infection or a specific condition such as peripheral or central nervous system lesions * Neoplasm; diabetes mellitus or osteonecrosis * Any mental disorder that may make it difficult to adapt to exercise

Design outcomes

Primary

MeasureTime frameDescription
Constant-Murley Score1. At the end of the treatment 2. The second evaluation: Six weeks after the first one (6th week post-treatment) 3. The last evaluation: Three months after the second one (18th week post-treatment)The primary outcome was shoulder global function which was measured by the Constant-Murley score (CMS). The questionnaire assesses four shoulder functions: 1) pain; 2) activities of daily living (sleeping, work, leisure); 3) range of motion; and 4) muscle strength. The total score ranges from 0 to 100, with a higher score indicating better shoulder function.

Secondary

MeasureTime frameDescription
Visual Analogue ScaleVisual analogue scale was recorded at the end of the treatment, at 6-weeks and 18-weeks post-treatmentThe secondary outcome was pain which was measured by the visual analogue scale. The patients themselves used the VAS to make an assessment of their pain with 0 representing no pain, 10 cm representing severe pain.
Disabilities of the Arm, Shoulder and Hand (DASH) ScoreDisabilities of the Arm, Shoulder and Hand (DASH) Score was recorded at the end of the treatment, at 6-weeks and 18-weeks post-treatmentOne of the secondary outcome was disability which was measured by the Disabilities of the Arm, Shoulder and Hand (DASH) Score. The DASH consists mainly of a 30-item disability/symptom on a 5-point Likert scale, scored 0 (no disability) to 100 (maximum disability).

Countries

Turkey (Türkiye)

Participant flow

Recruitment details

35 who met the study inclusion criteria were randomly separated into two groups: the interferential current group (n = 18) and the sham group (n =17).

Pre-assignment details

18 patients were excluded * Rheumatic diseases, 6 * Multiple trauma, 5 * Cerebrovasculer diseases, 3 * Peripheral nerve injury, 2 * Shoulder subluxation, 2

Participants by arm

ArmCount
Rehabilitation and Interferential Current Therapy
In this arm, interferential current therapy was applied to the patients in addition to the rehabilitation program. Interferential current: were applied to the patients before the each exercise session. Pre-modulated bipolar method with the currier frequency of 4 kHz by a combination therapy unit (Sonopuls 692, Enraf-Nonius) with two electrodes (8×6 cm) was used. One electrode was placed on the lateral part of the deltoid muscle; the other was placed on the trapezium muscle close to the shoulder. Subjects were told that in order to produce an effect, the intensity of the stimulator must be maintained at a strong but comfortable level at all times. Rehabilitation program: Rehabilitation program carried out under the guidance of same physiotherapist 3 times a week for 6 weeks. At the end of 6 weeks', the physiotherapist described the home training program involving the resistance exercises by using therabands
18
Rehabilitation and Sham Therapy
In this arm, sham interferential current therapy was applied to the patients in addition to the rehabilitation program. Sham interferential current were applied to the patients before the each exercise session. Pre-modulated bipolar method with the currier frequency of 4 kHz by a combination therapy unit (Sonopuls 692, Enraf-Nonius) with two electrodes (8×6 cm) was used. One electrode was placed on the lateral part of the deltoid muscle; the other was placed on the trapezium muscle close to the shoulder. The sham interferential current therapy consisted of the placement of the same pads for the same time but no electrical stimulation was applied to the probes. Rehabilitation program: Rehabilitation program carried out under the guidance of same physiotherapist 3 times a week for 6 weeks. At the end of 6 weeks', the physiotherapist described the home training program involving the resistance exercises by using therabands.
17
Total35

Baseline characteristics

CharacteristicRehabilitation and Interferential Current TherapyRehabilitation and Sham TherapyTotal
Age, Continuous58.9 years
STANDARD_DEVIATION 10.7
62.0 years
STANDARD_DEVIATION 9.5
60.4 years
STANDARD_DEVIATION 10.1
Anatomic segment of proximal humerus fracture
Greater tuberosity and Surgical neck fracture
11 Participants9 Participants20 Participants
Anatomic segment of proximal humerus fracture
Greater tuberosity fracture
5 Participants3 Participants8 Participants
Anatomic segment of proximal humerus fracture
Surgical neck fracture
2 Participants5 Participants7 Participants
Body mass index28.0 kg/m^2
STANDARD_DEVIATION 3.2
30.8 kg/m^2
STANDARD_DEVIATION 5.6
29.3 kg/m^2
STANDARD_DEVIATION 4.7
Fracture side
Left fracture
3 Participants2 Participants5 Participants
Fracture side
Right fracture
15 Participants15 Participants30 Participants
Neer classification
Type-1 Neer Classification
4 Participants2 Participants6 Participants
Neer classification
Type-2 Neer Classification
3 Participants6 Participants9 Participants
Neer classification
Type-3 Neer Classification
11 Participants9 Participants20 Participants
Region of Enrollment
Turkey
18 participants17 participants35 participants
Sex: Female, Male
Female
12 Participants11 Participants23 Participants
Sex: Female, Male
Male
6 Participants6 Participants12 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 180 / 17
other
Total, other adverse events
0 / 180 / 17
serious
Total, serious adverse events
0 / 180 / 17

Outcome results

Primary

Constant-Murley Score

The primary outcome was shoulder global function which was measured by the Constant-Murley score (CMS). The questionnaire assesses four shoulder functions: 1) pain; 2) activities of daily living (sleeping, work, leisure); 3) range of motion; and 4) muscle strength. The total score ranges from 0 to 100, with a higher score indicating better shoulder function.

Time frame: 1. At the end of the treatment 2. The second evaluation: Six weeks after the first one (6th week post-treatment) 3. The last evaluation: Three months after the second one (18th week post-treatment)

ArmMeasureGroupValue (MEAN)Dispersion
Rehabilitation and Interferential Current TherapyConstant-Murley ScorePost treatment (Constant-Murley scores)57.0 score on a scaleStandard Deviation 7.7
Rehabilitation and Interferential Current TherapyConstant-Murley Score6th week post-treatment (Constant-Murley scores)69.0 score on a scaleStandard Deviation 8.9
Rehabilitation and Interferential Current TherapyConstant-Murley Score18th week post-treatment (Constant-Murley scores)79.6 score on a scaleStandard Deviation 9.4
Rehabilitation and Sham TherapyConstant-Murley ScorePost treatment (Constant-Murley scores)48.2 score on a scaleStandard Deviation 12
Rehabilitation and Sham TherapyConstant-Murley Score6th week post-treatment (Constant-Murley scores)60.7 score on a scaleStandard Deviation 12.1
Rehabilitation and Sham TherapyConstant-Murley Score18th week post-treatment (Constant-Murley scores)69.3 score on a scaleStandard Deviation 14.2
Secondary

Disabilities of the Arm, Shoulder and Hand (DASH) Score

One of the secondary outcome was disability which was measured by the Disabilities of the Arm, Shoulder and Hand (DASH) Score. The DASH consists mainly of a 30-item disability/symptom on a 5-point Likert scale, scored 0 (no disability) to 100 (maximum disability).

Time frame: Disabilities of the Arm, Shoulder and Hand (DASH) Score was recorded at the end of the treatment, at 6-weeks and 18-weeks post-treatment

ArmMeasureGroupValue (MEAN)Dispersion
Rehabilitation and Interferential Current TherapyDisabilities of the Arm, Shoulder and Hand (DASH) ScoreDASH score at post-treatment28 score on a scaleStandard Deviation 11
Rehabilitation and Interferential Current TherapyDisabilities of the Arm, Shoulder and Hand (DASH) ScoreDASH score at 6-weeks post-treatment15.3 score on a scaleStandard Deviation 9.2
Rehabilitation and Interferential Current TherapyDisabilities of the Arm, Shoulder and Hand (DASH) ScoreDASH score at 18-weeks post-treatment7.7 score on a scaleStandard Deviation 7.3
Rehabilitation and Sham TherapyDisabilities of the Arm, Shoulder and Hand (DASH) ScoreDASH score at post-treatment38.4 score on a scaleStandard Deviation 17.5
Rehabilitation and Sham TherapyDisabilities of the Arm, Shoulder and Hand (DASH) ScoreDASH score at 6-weeks post-treatment23.3 score on a scaleStandard Deviation 13
Rehabilitation and Sham TherapyDisabilities of the Arm, Shoulder and Hand (DASH) ScoreDASH score at 18-weeks post-treatment12.5 score on a scaleStandard Deviation 11.3
Secondary

Visual Analogue Scale

The secondary outcome was pain which was measured by the visual analogue scale. The patients themselves used the VAS to make an assessment of their pain with 0 representing no pain, 10 cm representing severe pain.

Time frame: Visual analogue scale was recorded at the end of the treatment, at 6-weeks and 18-weeks post-treatment

ArmMeasureGroupValue (MEAN)Dispersion
Rehabilitation and Interferential Current TherapyVisual Analogue ScaleVAS at the post-treatment3.9 score on a scaleStandard Deviation 1.5
Rehabilitation and Interferential Current TherapyVisual Analogue ScaleVAS at 6-weeks post-treatment2.0 score on a scaleStandard Deviation 1.7
Rehabilitation and Interferential Current TherapyVisual Analogue ScaleVAS at 18-weeks post-treatment0.7 score on a scaleStandard Deviation 1.1
Rehabilitation and Sham TherapyVisual Analogue ScaleVAS at the post-treatment4.7 score on a scaleStandard Deviation 1.5
Rehabilitation and Sham TherapyVisual Analogue ScaleVAS at 6-weeks post-treatment3.0 score on a scaleStandard Deviation 1.5
Rehabilitation and Sham TherapyVisual Analogue ScaleVAS at 18-weeks post-treatment1.7 score on a scaleStandard Deviation 1.4

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