Skip to main content
OpenTrials
Completed

NCT Number: NCT06229028

Examining the Effects of Patient Information Forms, Exercise Forms and Video Recordings

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pamukkale University

Merkez, Denizli, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

hand rehabilitation with verbal explanation

Other

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

Other

hand rehabilitation with patient information and exercise forms

hand rehabilitation with video recording

Other

hand rehabilitation with video recording

Primary outcomes

  1. Impact of Event Scale-Revised

    Time frame: 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.

    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.

  2. State-trait Anxiety Inventory

    Time frame: 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.

    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).

Secondary outcomes

  1. Grip and Pinch Strength

    Time frame: 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.

    Grip and Pinch Strength strength is measured in pounds, kilograms by squeezing a dynamometer and a pinchmeter about three times in each hand.

  2. Michigan Hand Outcomes Questionnaire

    Time frame: 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.

    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.

Sponsors and collaborators

Lead sponsor

Pamukkale University

Other

Registry information

Official study title

Examining the Effects of Patient Information Forms, Exercise Forms and Video Recordings on Clinical and Functional Results in Patients With Hand and Forearm Injuries.

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jan 29, 2024
Registry last updated
Jul 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.