The Effect of Handgrip Strength on Functional Level

Sponsor
Suleyman Demirel University (Other)
Overall Status
Completed
CT.gov ID
NCT06072261
Collaborator
(none)
100
1
2
5
19.9

Study Details

Study Description

Brief Summary

In this study, it was aimed to examine the effects of kinesio tape applied to the forearm extensor muscles on the functional level of patients undergoing lower extremity surgery with walker ambulation.

Patients who were evaluated before being included in the post-surgical rehabilitation program (before kinesio tape application) and before discharge will be included in the study group. For the control group data, patients who underwent lower extremity surgery at the same institution for similar periods, but were included in the standard rehabilitation program, but did not apply kinesio tape, will be included. Standard rehabilitation practice includes in-bed transfer training, gait training, practice of daily living activities, and therapeutic exercise practices .

Before the standard rehabilitation program, kinesio taping was applied to both upper extremities in the form of a "Y" tape from the medial epicondyle to the wrist flexors, with 15-20% tension, to the patients hospitalized in the orthopedic service after lower extremity surgery. The tape should remain on the patient's arm throughout the hospital stay

Condition or Disease Intervention/Treatment Phase
  • Other: kinesio tape application
N/A

Detailed Description

In the literature, as predictors of poor functional recovery after lower extremity fracture and prosthetic surgery; old age, low functional level before fracture, cognitive impairment, comorbidities, living alone, and long hospital stay have been shown. Although the lower extremity has a higher relationship than the upper extremity in activities such as walking and physical function, the grip strength, which is closely related to the lower extremity strength, is an easily measurable, reliable, and applicable method for assessing whole body strength.In addition, handgrip strength is used as an important criterion in determining the functional level of elderly individuals. Although there are many studies in the literature that grip strength is a determinant of functional level, no study has been encountered showing the effects of kinesio taping application on the functional level of improving grip strength in elderly individuals who have undergone lower extremity surgery and provided with walker assisted ambulation.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
The Effect of Handgrip Strength on Functional Level in Elderly People Having Lower Extremity Surgery
Actual Study Start Date :
Apr 15, 2023
Actual Primary Completion Date :
Aug 1, 2023
Actual Study Completion Date :
Sep 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Kinesio Tape Group

Before the standard rehabilitation program, kinesio taping was applied to both upper extremities in the form of a "Y" tape from the medial epicondyle to the wrist flexors, with 15-20% tension, to the patients hospitalized in the orthopedic service after lower extremity surgery. The tape should remain on the patient's arm throughout the hospital stay

Other: kinesio tape application
Before the standard rehabilitation program, kinesio taping was applied to both upper extremities in the form of a "Y" tape from the medial epicondyle to the wrist flexors, with 15-20% tension, to the patients hospitalized in the orthopedic service after lower extremity surgery. The tape should remain on the patient's arm throughout the hospital stay

No Intervention: Control Group

For the control group data, patients who underwent lower extremity surgery at the same institution for similar periods, but were included in the standard rehabilitation program, but did not apply kinesio tape, will be included. Standard rehabilitation practice includes in-bed transfer training, gait training, practice of daily living activities, and therapeutic exercise practices

Outcome Measures

Primary Outcome Measures

  1. Handgrip strenght [3-5 days (Change from Baseline Handgrip strenght at discharged)]

    It was evaluated using a Jamar handheld dynamometer. During the evaluation, the patient was asked to stand in a static position. Maximum grip strength measurements were performed with the elbow flexed at 90° in the patient sitting position. Measurements were repeated 3 times at 30 second intervals in both extremities, and the results were recorded in kilogram-force form. In the measurement of maximum handgrip strength, the participants were asked to continue squeezing even if there was pain, and the maximum grip strength they reach was recorded

  2. Pain assessment [3-5 days (Change from Baseline Handgrip strenght at discharged)]

    Visual Analogue Scale (VAS) was used for pain assessment. The pain of the patient, who determines a point on the vertically drawn line with a length of 10 cm, is determined over one hundred points. A score of 100 means unbearable pain, and a score of 0 means no pain at all. This evaluation provides information about the pain profile of patients during activity and at rest

  3. Functional Independence Measurement-FIM [3-5 days (Change from Baseline Handgrip strenght at discharged)]

    The FIM instrument FIM indicates the degree of independence of the individual in basic physical and cognitive activities in daily life. The FIM includes 18 items that measure functional independence in 6 subscales: self-care, sphincter control, mobility, locomotion, communication, and social cognition. Each item is rated on a seven-point scale that represents different gradations of independence and reflects the amount of assistance the patient requires to perform a specific activity. Independence is categorized and scored as complete independence, 7; modified independence, 6; requires supervision or setup, 5; requires minimal contact assistance, 4; requires moderate assistance, 3; requires maximal assistance, 2; and requires total assistance, 1. The sum of all 18 items comprises the patient's total FIM score, which ranges from 18 to 126

  4. Iowa Level of Assistance Scale (ILAS) and Walking Speed Scale (IWSS) [3-5 days (Change from Baseline Handgrip strenght at discharged)]

    ILAS and IWSS are a measurement method that evaluates various physical functions and whose validity and reliability have been demonstrated in patients with knee replacement. With the ILAS, the performance level of 4 different physical activities (from lying on the back to sitting, getting up from sitting, walking 4.57 meters (15 feet), going up and down three flights of stairs) is evaluated. The scoring of these physical activities is based on the level of assistance that patients need during the activities ("0" could not be tested, "1" unsuccessful, "2" maximum assistance, "3" medium assistance, "4" minimum assistance, "5" observational assistance, "5" observational assistance. 6" independent) are made. With IWSS, walking speed is evaluated at a distance of 13.4 meters (44 feet). This scale ranges from 0 to 6 ("0" ≤20 sec, "1" 21-30 sec, "2" 31-40 sec, "3" 41-50 sec, "4" 51-60 sec, "5" 61 -70 sec, "6" >70 sec) or the time to complete walking is recorded as a score.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients over 65 years of age of both sexes, patients who were followed up postoperatively in the Department of Orthopedics of Süleyman Demirel University, patients whose mobilization was provided with a walker, and patients whose general condition was oriented and cooperative, were included in the study
Exclusion Criteria:
  • Patients with uncontrollable lung or cardiac problems, patients with psychiatric disease (dementia…) that may affect the answers given, patients who used any drugs and alcohol that could affect cognitive functions were excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Menekşe ŞAFAK Merkez Isparta Turkey 32000

Sponsors and Collaborators

  • Suleyman Demirel University

Investigators

  • Principal Investigator: Zeliha BAŞKURT, Prof. Dr., Süleyman Demirel Üniversitesi
  • Study Chair: Ferdi BAŞKURT, Prof. Dr., Süleyman Demirel Üniversitesi
  • Study Chair: Tuba İNCE PARPUCU, Assist. Prof., Süleyman Demirel Üniversitesi

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Menekse Safak, Research Assistant, Suleyman Demirel University
ClinicalTrials.gov Identifier:
NCT06072261
Other Study ID Numbers:
  • MS2023/02
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 10, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Menekse Safak, Research Assistant, Suleyman Demirel University

Study Results

No Results Posted as of Oct 10, 2023