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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06229028
Other study ID # E-60116787-020-468698
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 8, 2024
Est. completion date June 8, 2024

Study information

Verified date January 2024
Source Pamukkale University
Contact HANDE USTA, PhD
Phone +905068209000
Email husta@pau.edu.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators believe that these information forms, exercise forms and video recordings that provide patient education will contribute to the collaborative approach of the patient and the clinician, the patient's participation in the treatment, the expectation of treatment and results, and their autonomy. The contribution of patient information forms, exercise forms and video recordings, which have become very important in recent years, to different degrees of results will be questioned.


Description:

Written and visual information can affect outcome measurements in health care. In addition to verbal information and guidance, written and visual information is also frequently recommended. This information increases patients' clinical knowledge, communication, and satisfaction and reduces potential anxiety. Forms have been created in various medical fields to inform the patient about medications, applications, and possible risks, and there are many studies on these instruction forms. The effectiveness of patient information forms and exercise forms in physiotherapy and occupational therapy has gained importance in recent years. It is used in areas such as athlete rehabilitation, impingement syndrome, and osteoarthritis. However, only one study was found, especially in the field of hand rehabilitation. The aim of planning this study is to examine the contribution of patient information forms, exercise forms, and video recordings to the clinical and functional results of patients who suffered hand and forearm injuries as a result of a work accident.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date June 8, 2024
Est. primary completion date May 8, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - who have a hand or forearm injury as a result of a work-related injury - who has undergone primary surgery/conservative treatment related to the injury - who is literate - who has and can use technological equipment to use visual and audio communication materials (video) Exclusion Criteria: - who miss the evaluations - who wants to leave the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
hand rehabilitation with verbal explanation
Patients in all groups will undergo a 12-week hand rehabilitation process that includes the use of appropriate orthoses if necessary, approaches to edema and pain, restoration of joint range of motion, strengthening, and functional return to work or activities. The application of the rehabilitation process will change according to the assigned group.
hand rehabilitation with patient information and exercise forms
hand rehabilitation with patient information and exercise forms
hand rehabilitation with video recording
hand rehabilitation with video recording

Locations

Country Name City State
Turkey Pamukkale University Merkez Deni?zli?

Sponsors (1)

Lead Sponsor Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Abu Abed M, Himmel W, Vormfelde S, Koschack J. Video-assisted patient education to modify behavior: a systematic review. Patient Educ Couns. 2014 Oct;97(1):16-22. doi: 10.1016/j.pec.2014.06.015. Epub 2014 Jul 5. — View Citation

Barton CJ, Rathleff MS. 'Managing My Patellofemoral Pain': the creation of an education leaflet for patients. BMJ Open Sport Exerc Med. 2016 Mar 31;2(1):e000086. doi: 10.1136/bmjsem-2015-000086. eCollection 2016. — View Citation

Snyder-Ramos SA, Seintsch H, Bottiger BW, Motsch J, Martin E, Bauer M. Patient satisfaction and information gain after the preanesthetic visit: a comparison of face-to-face interview, brochure, and video. Anesth Analg. 2005 Jun;100(6):1753-1758. doi: 10.1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Impact of Event Scale-Revised This scale is a 22-item self-report measure that assesses subjective distress caused by traumatic events. Items are rated on a 5-point scale ranging from 0 ("not at all") to 4 ("extremely"). The total score ranges from 0 to 88. A higher score indicates more affection for the traumatic event. The evaluation were completed in the first session when the patient applied to the hand rehabilitation unit, and it was also repeated at 3th months after the surgery or conservative treatment.
Primary State-trait Anxiety Inventory This inventory was developed by Spielberger et al. (1970) to measure anxiety from the perspective of states vs. traits. The state measurement assesses how the individual feels "right now" or at this moment. The range of possible scores is from a minimum score of 20 to a maximum score of 80. Scores are commonly classified as "no or low anxiety" (20-37), "moderate anxiety" (38-44), and "high anxiety" (45-80). The evaluation were completed in the first session when the patient applied to the hand rehabilitation unit, and it was also repeated at 3th months after the surgery or conservative treatment.
Secondary Grip and Pinch Strength Grip and Pinch Strength strength is measured in pounds, kilograms by squeezing a dynamometer and a pinchmeter about three times in each hand. The evaluation were completed in the first session when the patient applied to the hand rehabilitation unit, and it was also repeated at 3th months after the surgery or conservative treatment.
Secondary Michigan Hand Outcomes Questionnaire This Questionnaire is a tool used to assess patients with hand disorders through the measurement of 6 health domains: overall hand function, activities of daily living, pain, work performance, aesthetics, and patient satisfaction. An overall score can be obtained by summing the scores for all six scales after reversing the pain scale (pain=100-pain score) and then dividing by six. On the pain scale, high scores indicate greater pain, while on the other five scales, high scores denote better hand performance. The evaluation were completed in the first session when the patient applied to the hand rehabilitation unit, and it was also repeated at 3th months after the surgery or conservative treatment.
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