Trial Outcomes & Findings for The Effect of Biomechanical Scapular Mobilization With Movement and Motor Learning (NCT NCT04701814)

NCT ID: NCT04701814

Last Updated: 2022-05-18

Results Overview

1\. Visual Analogue Scale: was used to evaluate the intensity of pain, which The pain VAS is a continuous scale comprised of a horizontal (HVAS) or vertical (VVAS) line, usually, 10 centimetres in length, anchored by 2 verbal descriptors, one for each symptom extreme. For pain intensity, the scale is most commonly anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 10 centimetres).

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

38 participants

Primary outcome timeframe

3 weeks

Results posted on

2022-05-18

Participant Flow

Participant milestones

Participant milestones
Measure
Group A (Controlled Group)
received passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM) exercises, strengthen of rotator cuff, biceps, shoulder and scapular muscles, ultrasound (5 min. - 1.5 W/c.m2 - 1 MHZ), electrical stimulation ( interferential bipolar technique for 20 min. on shoulder joint). This treatment was repeated three times per weeks with 24 hours rest for 3 weeks.
Group B(Study Group)
All patients in group B received same treatment as group A with adding biomechanical scapular mobilization with movement and motor learning. biomechanical scapular mobilization with movement and motor learning: the therapist applied posterior tilt and exteral rotation with upward rotation mobilization to scapula and therapist also warp bilt around GH joint to applied inferior and posterior glid then ask patient to elevate his arm. then we applied motor learning approach by asking patient to elevate his arm with maintaining of external rotation with posterior glid of scapula.
Overall Study
STARTED
20
18
Overall Study
COMPLETED
15
15
Overall Study
NOT COMPLETED
5
3

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Group A (Controlled Group)
n=15 Participants
received passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM) exercises, strengthen of rotator cuff, biceps, shoulder and scapular muscles, ultrasound (5 min. - 1.5 W/c.m2 - 1 MHZ), electrical stimulation ( interferential bipolar technique for 20 min. on shoulder joint). This treatment was repeated three times per weeks with 24 hours rest for 3 weeks.
Group B(Study Group)
n=15 Participants
All patients in group B received same treatment as group A with biomechanical scapular mobilization with movement and motor learning. biomechanical scapular mobilization with movement and motor learning: the therapist applied posterior tilt and exteral rotation with upward rotation mobilization to scapula and therapist also warp bilt around GH joint to applied inferior and posterior glid then ask patient to elevate his arm. then we applied motor learning approach by asking patient to elevate his arm with maintaining of external rotation with posterior glid of scapula.
Total
n=30 Participants
Total of all reporting groups
Age, Categorical
<=18 years
0 Participants
n=15 Participants
0 Participants
n=15 Participants
0 Participants
n=30 Participants
Age, Categorical
Between 18 and 65 years
15 Participants
n=15 Participants
15 Participants
n=15 Participants
30 Participants
n=30 Participants
Age, Categorical
>=65 years
0 Participants
n=15 Participants
0 Participants
n=15 Participants
0 Participants
n=30 Participants
Age, Continuous
35.1 weeks
STANDARD_DEVIATION 8.123 • n=15 Participants
35.3 weeks
STANDARD_DEVIATION 7.943 • n=15 Participants
35.2 weeks
STANDARD_DEVIATION 8 • n=30 Participants
Sex: Female, Male
Female
10 Participants
n=15 Participants
10 Participants
n=15 Participants
20 Participants
n=30 Participants
Sex: Female, Male
Male
5 Participants
n=15 Participants
5 Participants
n=15 Participants
10 Participants
n=30 Participants
Race and Ethnicity Not Collected
0 Participants
Race and Ethnicity were not collected from any participant.
Region of Enrollment
Egypt
15 Participants
n=15 Participants
15 Participants
n=15 Participants
30 Participants
n=30 Participants

PRIMARY outcome

Timeframe: 3 weeks

1\. Visual Analogue Scale: was used to evaluate the intensity of pain, which The pain VAS is a continuous scale comprised of a horizontal (HVAS) or vertical (VVAS) line, usually, 10 centimetres in length, anchored by 2 verbal descriptors, one for each symptom extreme. For pain intensity, the scale is most commonly anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 10 centimetres).

Outcome measures

Outcome measures
Measure
Group A (Controlled Group)
n=15 Participants
received passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM) exercises, strengthen of rotator cuff, biceps, shoulder and scapular muscles, ultrasound (5 min. - 1.5 W/c.m2 - 1 MHZ), electrical stimulation ( interferential bipolar technique for 20 min. on shoulder joint). This treatment was repeated three times per weeks with 24 hours rest for 3 weeks.
Group B(Study Group)
n=15 Participants
All patients in group B received same treatment as group A but adding biomechanical scapular mobilization with movement and motor learning to treatment. biomechanical scapular mobilization with movement and motor learning: the therapist applied posterior tilt and exteral rotation with upward rotation mobilization to scapula and therapist also warp bilt around GH joint to applied inferior and posterior glid then ask patient to elevate his arm. then we applied motor learning approach by asking patient to elevate his arm with maintaining of external rotation with posterior glid of scapula.
Visual Analogue Scale
4.2 score on a scale
Standard Deviation 1.474
0.9 score on a scale
Standard Deviation 1.280

PRIMARY outcome

Timeframe: 3 weeks

Universal goniometer: was used to measure the available range of motion at a joint. where used to measure an available range of motion of abduction and flexion of the shoulder joint.

Outcome measures

Outcome measures
Measure
Group A (Controlled Group)
n=15 Participants
received passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM) exercises, strengthen of rotator cuff, biceps, shoulder and scapular muscles, ultrasound (5 min. - 1.5 W/c.m2 - 1 MHZ), electrical stimulation ( interferential bipolar technique for 20 min. on shoulder joint). This treatment was repeated three times per weeks with 24 hours rest for 3 weeks.
Group B(Study Group)
n=15 Participants
All patients in group B received same treatment as group A but adding biomechanical scapular mobilization with movement and motor learning to treatment. biomechanical scapular mobilization with movement and motor learning: the therapist applied posterior tilt and exteral rotation with upward rotation mobilization to scapula and therapist also warp bilt around GH joint to applied inferior and posterior glid then ask patient to elevate his arm. then we applied motor learning approach by asking patient to elevate his arm with maintaining of external rotation with posterior glid of scapula.
Universal Goniometer
Abduction
85.7 Degree
Standard Deviation 9.083
130.9 Degree
Standard Deviation 8.302
Universal Goniometer
Flexion
131.7 Degree
Standard Deviation 10.761
173.4 Degree
Standard Deviation 6.544

Adverse Events

Group A (Controlled Group)

Serious events: 0 serious events
Other events: 1 other events
Deaths: 0 deaths

Group B(Study Group)

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Other adverse events
Measure
Group A (Controlled Group)
n=2 participants at risk
received passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM) exercises, strengthen of rotator cuff, biceps, shoulder and scapular muscles, ultrasound (5 min. - 1.5 W/c.m2 - 1 MHZ), electrical stimulation ( interferential bipolar technique for 20 min. on shoulder joint). This treatment was repeated three times per weeks with 24 hours rest for 3 weeks.
Group B(Study Group)
n=1 participants at risk
All patients in group B received same treatment as group A but adding biomechanical scapular mobilization with movement and motor learning to treatment. biomechanical scapular mobilization with movement and motor learning: the therapist applied posterior tilt and exteral rotation with upward rotation mobilization to scapula and therapist also warp bilt around GH joint to applied inferior and posterior glid then ask patient to elevate his arm. then we applied motor learning approach by asking patient to elevate his arm with maintaining of external rotation with posterior glid of scapula.
Musculoskeletal and connective tissue disorders
Shoulder Pain
50.0%
1/2 • Number of events 1 • 5 months
The study isn't including serious adverse events: Adverse events that are not Serious Adverse Events. the study is depend on manual therapy that its evidence base to occur any adverse effect is very low may be occur with manipulation technique more than mobilization. when we check the patients after technique to record any adverse events, we found nothing so there is no any adverse event. Also, we have not found any study recorded adverse event due to using mobilization technique in shoulder.
0.00%
0/1 • 5 months
The study isn't including serious adverse events: Adverse events that are not Serious Adverse Events. the study is depend on manual therapy that its evidence base to occur any adverse effect is very low may be occur with manipulation technique more than mobilization. when we check the patients after technique to record any adverse events, we found nothing so there is no any adverse event. Also, we have not found any study recorded adverse event due to using mobilization technique in shoulder.

Additional Information

P.T Moataz Abdelaal

Pharos university in Alexandria

Phone: 1060081213

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place