ALL Metrics
-
Views
-
Downloads
Get PDF
Get XML
Cite
Export
Track
Study Protocol
Clinical trial

Efficacy of scapular and upper limb proprioceptive neuromuscular facilitation techniques on scapular alignment, upper limb function, and gait in subacute stroke: a randomized controlled trial protocol

[version 1; peer review: awaiting peer review]
PUBLISHED 11 Oct 2023
Author details Author details
OPEN PEER REVIEW
REVIEWER STATUS AWAITING PEER REVIEW

This article is included in the Datta Meghe Institute of Higher Education and Research collection.

Abstract

Background: Stroke is a neurological disability produced by vascular-related acute focal injury to the central nervous system and is one of the leading causes of disability in adults, and it is frequently accompanied by motor skill loss. Patients suffering from hemiplegia after a stroke are more prone to have fall and are more likely to experience further injury due to irregular gait, diminished muscular strength, and functional impairment. In the affected upper limb of the hemiplegic stroke, spasticity in the shoulder girdle causes scapular malalignment, which reduces the functional mobility and stability of the upper limb. This is reflected as the reduced reciprocal arm swing during walking, which is further reinforced by an abnormal synergy pattern on the affected side. Proprioceptive neuromuscular facilitation (PNF) is a treatment strategy that stimulates motor activity and enhances control and function of the neuromuscular system. This research protocol is intended to assess and evaluate the effects of applying scapular and upper limb PNF along with conventional physiotherapy treatment to subacute-stroke patients on their scapular alignment, upper limb function, and gait.
Methods: A total of 40 individuals in total will be allocated equally into two groups, group-A (experimental) and group-B (control). Both groups will be receiving treatment for six weeks with five sessions per week. Each patient will be examined both before and after therapy using the Palpation Meter (PALM), the Fugl-Meyer Assessment of Upper Extremity (FMA-UE), 10-Meter Walk Test, Handheld dynamometer (10MWT), and Dynamic gait index (DGI). After six weeks of therapy, the results will be assessed and the data will be analyzed before and after the intervention using a paired t-test to discover within-group differences in measurements.
Conclusions: This physiotherapy method may be used in the management of stroke patients if our study's hypothesis is found to be valid.
Registration: CTRI (CTRI/2023/05/052930, 19/05/2023).

Keywords

Proprioceptive Neuromuscular Facilitation, Scapular Alignment, Upper Limb Function, Gait, hemiplegia, stroke, physiotherapy treatment

Introduction

Stroke is clinically defined as a neurological impairment caused by a vascular-related acute focal damage to the central nervous system (CNS).1 According to the World Health Organization (WHO), stroke has been reported as a major cause of disability and death worldwide, with an incidence between 0.2 and 2.5 per 1,000 people each year and in India the prevalence of stroke significantly increases with age, 0.80% at 45–54 years old and 1.97% at 55–69 years old.2 Stroke accounts for 60 to 80% of cases of upper extremity disability due to weakness of proximal muscles, causing severe disability in hand functions and gait, considered as a significant issue.3 Stroke patients have poor voluntary control, weakness, imbalance, and malalignment, all of which impede an affected arm's ability to maintain proper scapular orientation. These elements play a role in the 76% of stroke patients who exhibit an imbalance in scapular position and the 67% of those who exhibit aberrant scapular motions, both of which indicate impaired stability of the proximal upper extremity. To increase the upper extremity's limited functions and distal movement, it is crucial to achieve stability.4

Following a stroke there is loss of voluntary control in the flaccid stage, followed by spasticity, which affects the shoulder joint and produces changes to the scapulothoracic joint, which in turn impacts scapular malalignment.5 In the spastic stage, the flexor tone dominates, causing shoulder joint retraction, depression, and adduction. The latissimus dorsi, rhomboids, elevator scapulae, pectoralis major and minor, and can become hypertonic, causing the scapula to rotate even further downward. These muscles are crucial for the shoulder complex stability, which is necessary for the shoulder joint to have a proper range of motion. Mandalidis and O'Brien hypothesized that in order to regain the normal functioning of the upper extremity's distal joints, it is crucial to strengthen the scapular stabilizers.6

In the affected upper limb of the hemiplegic stroke, spasticity in the shoulder girdle causes scapular malalignment, which reduces the functional mobility and stability of the upper limb. This is reflected as the reduced reciprocal arm swing during walking, which is further reinforced by an abnormal synergy pattern on the affected side. According to Kelly et al., stroke patients walked more slowly than the general population, used more energy, and had shorter walking times.7

In current clinical practice, techniques like proprioceptive neuromuscular facilitation (PNF), motor re-learning programme (MRP), motor imagery technique, constraint-induced movement therapy (CIMT), robotic therapy, and neuromuscular stimulation techniques are used to help hemiplegic patients regain control of their upper limbs. In order to stimulate motor functions and enhance neuromuscular control and function, proprioceptive neuromuscular facilitation (PNF), a therapeutic exercise strategy, blends functionally oriented diagonal patterns with neuromuscular facilitation approaches. The main goal of exercises using the patterns of PNF is to increase functional mobility by inhibition, facilitation, strengthening, and relaxation of muscle groups. This technique of therapeutic exercise is distinguished by the utilization of diagonal patterns and the use of sensory cues—specifically proprioceptive, cutaneous, visual, and aural stimuli—to elicit or augment motor response.8,9

Scapular PNF is used in two diagonal directions: anterior elevation—posterior depression and posterior elevation—anterior depression. Techniques of scapular PNF can be utilized to target-stretch or target-strengthen specific muscles since they involve functional or diagonal patterns for exercising. These methods also assist the muscles in relearning the appropriate timing, and amount of activation in order to keep the balance between various muscle groups. Few studies have stated that scapular PNF was efficacious in improving the upper limb mobility, but the techniques were not clear.8,1012

Conventional physiotherapy includes exercises such as passive motion, active assisted exercises, active exercises, balance exercise, and gait training. Conventional exercises are ones that are practised globally. Ellenbecker et al., reported that the movement of one segment affected other proximal and distal parts. Several factors, such as muscular weakness and hypertonicity, have been known to restrict the functions of the limbs.13 Lai et al., reported that 55 to 80% of stroke patients with impaired upper limb functions even after six months of recovery after injury had permanent dysfunction in the performance of daily living activities.14 Wang reported that studies on the effectiveness of PNF-based treatment have been both supportive and conflicting and that very few studies on pelvic facilitation for gait improvement existed.9,12,15 Although there have been many studies using PNF for stroke, sports injuries, and musculoskeletal disorders.1619 Little research has been done on the effects of the intervention on the scapular movements and walking of stroke patients when it is applied to their scapular adductors. In this context, this study attempted to identify the effects of training using PNF along with conventional physiotherapy on the scapular alignment and upper limb function and gait velocity of stroke patients. The research question identified was whether scapular stabilization will improve upper limb function and gait velocity in subacute stroke patients?

Aims

The study’s aim is to find out the efficacy of scapular and upper limb proprioceptive neuromuscular facilitation techniques along with conventional therapy on subjects with sub-acute stroke in a randomized controlled trial (RCT) with two arms of parallel superiority/equivalence on improving scapular alignment, upper limb function and gait velocity. The end point results will be compared on a marginal basis to determine effectiveness.

Primary objectives

  • 1. To study the subjects with subacute stroke, treated with scapular and upper limb PNF techniques in addition to conventional therapy and its effect on gaining scapular alignment (measured by palpation meter), and upper limb function (measured by Fugl Meyer Assessment for Upper limb (FMA-UE)) and gait velocity (measured using 10 Meter walk test (10MWT)).

  • 2. To compare and evaluate the efficacy of scapular and upper limb PNF techniques along with conventional therapy over conventional physiotherapy for bringing on change in scapular alignment, upper limb function, and gait in sub-acute stroke.

Secondary objectives

  • 1. To study the subjects with subacute stroke treated with scapular and upper limb proprioceptive neuromuscular facilitation techniques along with conventional therapy on improving hand grip strength using handheld dynamometer.

  • 2. To study the subjects with subacute stroke treated with scapular and upper limb PNF techniques in addition to conventional therapy on improving gait and balance using dynamic gait index (DGI) over the population.

Trial design

This study is a single-centric, two arm parallel, open-label equivalence randomized controlled trial. This study has been registered with Clinical Trials Registry India (CTRI) (CTRI/2023/05/052930, 19/05/2023).

Protocol

This study protocol adheres to the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) checklist.20 The model consent form, data collection form and schedule of enrolment, interventions, and assessments can be found as Extended data.21 The study will be carried out in compliance with the principles of the Consolidated Standards of Reporting Trials (CONSORT) guidelines. Figure 1 provides a summary of the study process. After receiving approval from the Datta Meghe Institute of Higher Education and Research's institutional ethics committee (Institutional Ethical Clearance was obtained on 04/02/2023; IEC No. – DMIHER (DU)/IEC/2023/547), participants will be recruited from the Physiotherapy OPD of Acharya Vinoba Bhave Rural Hospital, Datta Meghe Institute of Higher Education and Research, Sawangi Meghe, Wardha, Maharashtra, using inclusion and exclusion criteria for the study. Subjects will be invited and screened as part of the study's inclusion process. Following the screening, participants will be educated about the study and given a written informed consent form. After consent is obtained, the assessor will conduct the baseline assessment using the questionnaire. Then, the study's participants will be subsequently subdivided into two groups.

84c534a6-e4e8-4a88-bd12-fb2ac12866b1_figure1.gif

Figure 1. Summary of study process.

For subject allocation, a randomization procedure utilizing a computer-generated list will be used. Randomization for 1:1 allocation of Group-A (PNF) and Group-B (Conventional therapy) with the goal to treat. When engaging participants, the inclusion and exclusion criteria for selection will be based on the cut-off values at baseline parameters. Throughout the six-month recruitment phase, a secondary source of recruiting will be used if more study participants are needed. PNF and conventional therapy will be given to the active group to evaluate the improvement in scapular alignment, upper limb function, and gait velocity at endpoint results in marginal difference, whereas control group will only receive conventional therapy. As conventional physiotherapy is already proven and a novel approach to be proven should be compared with the universal one.

Participants will be enrolled and evaluated at pre-post treatment, including visits one and two for subject enrolment and screening, baseline and after the conclusion of six weeks, when primary and secondary parameters will be measured. The study schedule of enrolment, intervention and assessment of study (as recommended by the SPIRIT guidelines) is illustrated in Figure 2.

84c534a6-e4e8-4a88-bd12-fb2ac12866b1_figure2.gif

Figure 2. Schedule of enrolment, interventions, and assessments.

Inclusion criteria

  • 1. Patients with hemiplegic subacute stroke, any gender aged between 50 and 70 years old.

  • 2. Patients with more than 24 in Mini-mental state examination.

  • 3. Patients with spasticity between grades (+1 and 1) on the Modified Ashworth Scale (MAS).

  • 4. Patients with Brunnstrom Voluntary control grading more than or equal to four.

  • 5. Patients who could walk independently, either with or without assistance.

Exclusion criteria

  • 1. Patients who have heart failure symptoms, uncontrolled hypertension, or unstable angina.

  • 2. Patients who have a recurrent stroke.

  • 3. Patients who have any traumatic upper and lower limb musculoskeletal conditions.

  • 4. Patients who had organ damage such as lung, heart, kidney, or liver failure.

Interventions

Groups

Group A: Experimental group

Group B: Control group

Experimental group

After screening and randomization, the experimental group will receive scapular PNF coupled with upper limb PNF and conventional physiotherapy treatment.

PNF will be applied to the scapula and upper limb in both D1 and D2 flexion and extension patterns of the patients in side-lying and sitting position. Table 1 shows the PNF pattern of each segment. The techniques will be initiated using rhythmic initiation then progressing to combinations of isotonics, dynamic reversal, rhythmic stabilization, contract relax and hold relax techniques of PNF. These techniques will be performed for 60 minutes/day, five days/week, for six weeks. Ample amount of rest periods will be given in-between to prevent fatigue.8,10

Table 1. Showing the PNF pattern of each segment of upper limb.

SegmentSynergy PatternPNF Pattern
ScapulaRetracted/DepressedD1 Flexion/D2 Flexion
GlenohumeralAdduction/Internal RotationD2 Flexion
elbowFlexionD1 Extension
forearmPronationD1 Flexion/D2 Flexion
wristFlexionD1 Extension/D2 Flexion
fingersFlexionD1 Extension/D2 Flexion

Conventional physiotherapy treatment includes closed kinematic chain exercises of upper limb, upper and lower extremity range of motion exercises, stretching and strengthening exercises for upper limb, trunk and lower limb, balance & coordination, manual dexterity exercises (e.g., grasp release), and teaching of activities of daily living (ADLs), according to the patient’s needs.22 It will be performed for 60 minutes/day, five days/week, for six weeks.16,23,24

Control group

After screening and randomization, the control group will receive conventional physiotherapy treatment. It includes closed kinematic chain exercises of upper limb, upper and lower extremity range of motion exercises, stretching and strengthening exercises for upper limb, trunk and lower limb, balance & coordination, manual dexterity exercises (e.g., grasp release), and teaching of ADLs, according to patient’s needs. It will be performed for 60 minutes/day, five days/week, for six weeks.16,23,24

Criteria for discontinuing allocated interventions for a given trial participant

If any patients in any of the allocated groups develop complications (e.g., complex regional pain syndrome), their participation in the study will be discontinued. The patients will then receive appropriate care and offered outpatient rehabilitation as needed. Study participants will be retained in the trial (unless they withdraw their consent) to enable follow-up data collection and to prevent missing data.

Adherence and concomitant care

During the first consultation, the importance of following the study guidelines and adhering to the allocated group will be highlighted. Exercise adherence will be recorded as a percentage of completed exercises during the first follow up (after the six-week intervention) for both groups. Exercise adherence will be taken into consideration when performing the per-protocol analysis.

All enrolled patients will be encouraged to contact the principal investigator directly, if experiencing problems related to their allocated group intervention. The principal investigator will then fill out a standardized form at these calls. Patients can use medicines and nutritional products as needed, prescribed by their physician after the episode of stroke. To avoid study-contamination, patients will be asked to adhere to the allocated rehabilitation intervention and not to seek alternative health-care services during the course of the study. Patients will be advised to contact their general practitioner or the principal investigator as needed.

Outcomes

Primary outcomes

Change in palpation meter (PALM) score

A palpation meter is a dependable tool for measuring both the angles and distance of scapula. The tool is used to record the horizontal distance of scapula from spine, two measurements will be taken: the horizontal distance from the root of the spine of the scapula to the spinous process of thoracic spine(T2), and from the inferior angle of the scapula to the spinous process of thoracic spine(T7). The vertical distance of scapula will be measured from the postero-inferior angle of the acromion to spinous process of cervical spine (C7). The angles measurement will be taken from the superior angle of the two scapula and inferior angles of the two scapula. The end of one arm of the calliper will be positioned over one of the landmarks, and the end of the other arm position over another landmark. The PALM inclinometer will be level for measurement of the horizontal distance between the scapula and the thoracic spine. The inclinometer value will be used to calculate the vertical distance between the scapula and C7. A reading will be taken from both the sides, and the variances in each position will be calculated.25 When there is a bilateral disparity in scapular distance that is greater than 1.0 cm to 1.5 cm, the scapular alignment is considered inappropriate or disturbed. A positive result suggests an upward scapular rotation, while a negative result shows a downward scapular rotation.2628

Change in Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score

It assesses and monitors recovery in hemiplegic patients following a stroke. The FMA-UE is one of the most commonly used tools for quantifying post-stroke upper limb impairment and rehabilitation. It is a condition-specific consequence that pertains to upper limb hemiparesis in stroke patients. Scale items are assessed based on their ability to execute the item using a 3-point ordinal scale, where 0 means cannot perform, 1 means partially performs, and 2 means fully performs. A total score is derived by adding all calculated item scores with a point range of 0-126.29

Change in 10-Meter Walk Test (10MWT) score

It measures the velocity of walking in meters per second over a short period of time. To the nearest tenth of a second, the total amount of time needed to walk 6 meters (m) will be recorded. Then, 6 m will be converted to m/s by dividing it by the whole amount of time it took to ambulate (in seconds).30 Normal Walking Speed m/s - Household Ambulator <0.40 m/s; Limited Community Ambulator 0.40 to <0.80 m/s; Community Ambulator ≥0.80 m/s.31

Secondary outcomes

Change in Hand Grip Strength (HGS) score (Handheld Dynamometer)

A handheld dynamometer will be used to measure HGS. The maximum value (in kg) will be obtained after the test is done three times with at least two minutes of rest in between.32

Change in DGI score

The DGI evaluates a participant's ability to maintain walking balance while responding to a variety of task demands in a variety of dynamic contexts. It is a useful test for those with vestibular and balance problems, as well as those who are at risk of falling. Each item is evaluated from 0 to 3, with 3 representing normal performance and 0 representing significant impairment. A DGI score of 24 is the highest possible. A total score of less than 19/24 is indicative of geriatric falls. A score of >22 signifies a safe ambulator.33

Sample size calculation

By using a power analysis with a 90% power and 5% Type 1 error determined for the primary variable, we determined the sample size.11

Sample size calculation formula using mean difference

n1=n2=2Zα+Zβ2σ2δ2

Primary variable (FMA-UE)

Mean ± SD (Pre) result on FMA-UE for experimental group in stroke patients = 17.93 ± 5.22.

Mean ± SD (Post) result on FMA-UE for Experimental group in stroke patients = 25.40 ± 4.34

Difference = 7.47

Considering estimated std.dev = 7

N1=21.96+1.2827.472/72=18

Total samples required = 18 per Group.

Considering 10% drop out = 2

Total sample size required = 20 per group

Total sample size required (N) = 2*20 = 40

Notations:

Zα=1.96
α=TypeIerrorat5%
Zβ=1.281β=Powerat90%
σ=std.dev=7

Data collection and management

The evaluation data will be obtained from a pre-established spreadsheet with variable baseline characteristics. Research data will be placed in a secure database. Non-electronic records, such as hard copies of assessment forms, signed informed consent forms, etc., will be stored safely in the study setting. A complete backup of the data entries will be performed every month until trial completion.

Data collection and reporting will be carried out under the supervision of the principal investigators. The research reports must be carefully checked for accuracy. The Excel spreadsheet will be published at the conclusion of the study and given to the statistician for the required analysis. Checklists can be used to avoid lost data due to incorrect staff procedures.

Participant retention and completion of follow-up assessments are expected to be relatively high due to the comprehensive follow-up assessment of this trial. Patients included in this trial are invited to follow-up assessments at six weeks.

Data analysis

The overall results will be calculated using R studio software 4.3 version. Data for the total participants in the study will be collected and will be organized with variables per participants record for their demographic and analysis assessment. Demographic variables such as age having quantitative measurement will be presented with mean, standard deviation, medium, maximum and minimum. While those qualitative or categorical will be presented with frequency and percentage such as hand dominance, gender and side affected. All the results for inferential statistics will be tabulated and tested at 5% level of significance (P<0.05). The primary outcome variables (PALM for measuring scapular alignment, FMA-UE for measuring upper limb function and 10MWT for measuring gait velocity) and secondary outcome variables (handheld dynamometer for measuring HGS and DGI for measuring balance and gait) will be tested for the pre-post results using paired t-test. Data will be subjected to normality test using Kolmogorov–Smirnov test. In cases of failed normality, a non-parametric test will be applied and if the data are normally distributed, a parametric test will be applied. For the paired t-test, a Wilcoxon paired signed rank test will be used. An unpaired t-test will be used to find the significant difference over the mean for both primary and secondary variables between control and experimental groups. A Mann–Whitney test will be used for the unpaired t-test. Association analysis for finding significance of cofounding parameters will be evaluated by using Chi-squared test or Fisher’s exact test or by using multi-variant analysis.

Monitoring

We will have a data monitoring committee for maintaining and integrating the data. The whole procedure is going to be held under the supervision of clinicians and departmental committee i.e., guide, head of department, principal, and member of the research guideline cell. Every month auditing trial going to be conduct. Any deviation from the protocol will be documented and will be addressed. The final dataset will be uploaded to institutional research website and will be accessible to concerned authorities.

Ethics and dissemination

This study has received approval from the Datta Meghe Institute of Higher Education and Research's institutional ethics committee (Institutional Ethical Clearance was obtained on 04/02/2023; IEC No. – DMIHER (DU)/IEC/2023/547). Planning to publish in an indexed journal and present the study at National Conference Proceedings.

Consent

Principal Investigator will obtain the informed consent from the patient on a printed form with signature and given the proof of confidentiality. The study program will be elaborated to the participant and one of their relatives, and principal investigator will take personal information as a part of procedure. The consent form will include the confidentiality statement and signatures of the principal investigator, patient and two witnesses. If required to disclose some information for the study, consent will be obtained from the patient with complete assurance of his/her confidentiality.

Confidentiality

All study-related information about the participants will be stored securely at the study site. Paper forms will in stored in locked cabinets, while electronic data will be stored on a password protected drive at the study site. Only persons involved in the trial will have access to the study-related information. Individual study information will not be released outside of the study without permission of the individual participant.

Ancillary and post-trial care

It is not expected that the allocated interventions will cause any harm to the participants. If any harm is caused, at the end of the 6-week intervention, the patients will be offered free-of-charge in- or outpatient rehabilitation as deemed clinically needed.

Access to the trial set

The principal investigator and the principal supervisor will have full access to the data set. The full-anonymized data set will be made available for the journal reviewing the manuscript.

Study status

The recruitment of participants is yet to be started.

Discussion

In normal human movement, voluntary movement patterns rely on synergies restricted by the CNS to operate together to produce an action. This movement may be impaired in stroke patients. As a result, the patient is unable to perform even the most basic movements. There is a mechanical coupling between the serratus anterior, trapezius, and rhomboids in the scapula that is disturbed after stroke, resulting in increased rhomboidal activity.34 When the movement is deliberately induced, this disturbance is obvious. During the flaccid period, the trunk tends to lean or shorten towards the hemiplegic side, causing the scapula to descend from its normal horizontal position. The trapezius and serratus anterior become flaccid as well, causing the scapula to rotate downward. The pectoralis major and minor, rhomboids, elevator scapulae, and latissimus dorsi might become hypertonic during the spastic period, further twisting the scapula downward.35 Many studies have found that glenohumeral and scapulothoracic strength training improves the functionality of the paretic upper extremities.3638

Mandalidis and O'Brien demonstrated that effective movement and range of motion of muscles functioning on a distal joint are only possible when the surrounding musculatures effectively stabilize the proximal joints.6,39 They claimed that strengthening the scapular stabilizers is crucial for restoring the upper extremity's distal joints function.

Kazi et al., (2023) performed a narrative review on scapular malalignment in patients with stroke. He included eight studies that were conducted on individuals in the acute, subacute, and chronic stages in the review. One acute, six chronic, two subacute, and chronic strokes were among them. In patients with acute, subacute, and chronic stroke, the findings indicated that scapular malalignment had an impact on the scapular balancing angle, functional hand mobility, and range of motion.40

Another study performed by Kim et al., (2017) examined upper limb function and gait ability in stroke patients when treated with scapular stabilization exercise during standing.38 Nine patients were placed in a study group and eight individuals were placed in a control group out of 17 hemiplegic patients following stroke. On the paretic side, the study group had physical therapy and scapular stabilization exercises. Prior to treatment, participants underwent an initial examination. To compare the changes, subjects were reassessed four and eight weeks later. Both gait abilities and hand function were measured. These findings suggested that scapular stability exercise while standing on an affected side for eight weeks had an impact on hemiplegic patients' capacity to walk and use their hands. Finding the best exercise for stroke patients with gait impairment and upper limb dysfunction will require more research.38

Moon et al., (2017) examined how stroke patients' scapular motions and walking abilities were affected by indirect application of PNF to the scapular adductor muscles. This study had five stroke patients who were enrolled as a single group. PNF patterns were administered to the scapulae anterior elevation and posterior depression patterns, as well as upper limb patterns, while the patients were in side laying and sitting positions. These findings imply that PNF training is useful in enhancing scapular motions and walking capability in stroke patients.8

When a literature search was conducted, only a small number of studies were found to focus on scapular PNF, and the available studies had been conducted on small populations and had methodological shortcomings.8,11,12 Scapular training was added to the therapy plan for stroke patients' upper limb rehabilitation and gait, although these trials were insufficient.38,41,42 As a result, there is a need to investigate the effect of scapular and upper limb PNF along with conventional therapy in subacute stroke on scapular alignment, upper limb function, and gait. The benefits of the study allow for a more tailored approach to the rehabilitation protocol as well as the flexibility to react to the patients' improving capacities throughout therapy.

Comments on this article Comments (0)

Version 1
VERSION 1 PUBLISHED 11 Oct 2023
Comment
Author details Author details
Competing interests
Grant information
Copyright
Download
 
Export To
metrics
Views Downloads
F1000Research - -
PubMed Central
Data from PMC are received and updated monthly.
- -
Citations
CITE
how to cite this article
Saklecha A, Quershi MI, Raghuveer R and Harjpal P. Efficacy of scapular and upper limb proprioceptive neuromuscular facilitation techniques on scapular alignment, upper limb function, and gait in subacute stroke: a randomized controlled trial protocol [version 1; peer review: awaiting peer review] F1000Research 2023, 12:1305 (https://doi.org/10.12688/f1000research.138133.1)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
track
receive updates on this article
Track an article to receive email alerts on any updates to this article.

Open Peer Review

Current Reviewer Status:
AWAITING PEER REVIEW
AWAITING PEER REVIEW
?
Key to Reviewer Statuses VIEW
ApprovedThe paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approvedFundamental flaws in the paper seriously undermine the findings and conclusions

Comments on this article Comments (0)

Version 1
VERSION 1 PUBLISHED 11 Oct 2023
Comment
Alongside their report, reviewers assign a status to the article:
Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions
Sign In
If you've forgotten your password, please enter your email address below and we'll send you instructions on how to reset your password.

The email address should be the one you originally registered with F1000.

Email address not valid, please try again

You registered with F1000 via Google, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Google account password, please click here.

You registered with F1000 via Facebook, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Facebook account password, please click here.

Code not correct, please try again
Email us for further assistance.
Server error, please try again.