ClinicalTrials.gg
CompletedNCT06117033Updated Nov 3, 2023

The Effect of Video-assisted Mobilisation Training on Mobility, Anxiety and Pain After Coronary Artery Bypass Surgery

An interventional study of video assisted mobilization training in Anxiety and Postoperative Pain, sponsored by Namik Kemal University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-11-03.

Sponsored by Namik Kemal University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Mar 2023, registered Oct 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study is a Randomized Controlled trial.The aim of this study was to investigate the effect of preoperative routine patient education and video-assisted mobilization training on postoperative mobility, anxiety level and pain in patients undergoing coronary artery bypass graft surgery.

Hypotheses of the study:

H1= Routine patient education and video-assisted mobilization training have an effect on postoperative anxiety level in patients undergoing coronary artery bypass graft surgery.

H2= Routine patient education and video-assisted mobilization training have an effect on postoperative mobility in patients undergoing coronary artery bypass graft surgery.

H3= Routine patient education and video-assisted mobilization training have an effect on postoperative pain in patients undergoing coronary artery bypass graft surgery.

Read the detailed description

This study is a Randomized Controlled trial. The study consists of 80 patients, 40 control and 40 study group. Patients in the experimental group who underwent coronary artery bypass graft surgery completed the "State Trait Anxiety Scale" in the preoperative period.

Then, video-assisted mobilization training was given together with routine patient training.After the patient underwent surgery, the "State Trait Anxiety Scale" was completed again before the first mobilization.After the first mobilization, "Patient Mobility Scale" and "Observer Mobility Scale" were completed."State Trait Anxiety Scale" was used again on the 2nd postoperative day before mobilization."Patient Mobility Scale" and "Observer Mobility Scale" were used after the patient was mobilized.

Patients in the control group who underwent coronary artery bypass graft surgery completed the "State Trait Anxiety Scale" in the preoperative period.Routine patient education was then given.After the patient underwent surgery, the "State Trait Anxiety Scale" was completed again before the first mobilization.After the first mobilization, "Patient Mobility Scale" and "Observer Mobility Scale" were completed. The "State Trait Anxiety Scale" was used again before mobilization on the 2nd postoperative day.After the patient was mobilized, "Patient Mobility Scale" and "Observer Mobility Scale" were used.

02

Conditions studied

  • Anxiety
  • Postoperative Pain

Keywords

  • coronary artery bypass graft
  • pain
  • mobility
  • anxiety
03

In context

Anxiety Disorders

5,063 studies on the registry are indexed under Anxiety Disorders; 1,408 are open to participants now.

This study's enrollment of 80 is close to the median of 80 across 4,339 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Namik Kemal University is the lead sponsor of 59 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients undergoing coronary artery bypass graft surgery,
  • Patients aged 18 years and older,
  • Patients who can speak Turkish,
  • Patients without a diagnosis of cognitive and psychiatric disorders that prevent them from expressing themselves,
  • Patients open to communication,
  • Patients who volunteered to participate in the study and gave verbal and written informed consent.

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (actual)

Study arms

  • Experimental
    experimental group

    Preoperative routine patient education and video-assisted mobilization training were given to patients undergoing coronary artery bypass graft surgery.

    Other: video assisted mobilization training

  • No intervention
    control group

    Patients in the control group received only routine patient education.

Interventions

  • Othervideo assisted mobilization training

    Preoperative video-assisted mobilization training was given to patients undergoing coronary artery bypass graft surgery

06

What researchers measure

Primary outcomes

  1. postoperative anxiety

    The effects of routine patient education and video-assisted mobilization training on postoperative anxiety in patients undergoing coronary artery bypass graft surgery were investigated. State Trait Anxiety Scale was used to measure the level of postoperative anxiety. The scale consists of two parts: "State Anxiety Scale" and "Trait Anxiety Scale". The State Anxiety Scale consists of a total of 20 statements. It defines the state anxiety of the individual. The individual is asked to express how he/she feels at a certain moment and under certain conditions, taking into account his/her feelings about that moment. There are 20 questions in the trait anxiety scale. It is asked to measure an individual's trait anxiety. The trait anxiety scale includes questions about how the individual usually feels. The total score value obtained from each scale is between 20-80. A high score indicates a high level of anxiety and a low score indicates a low level of anxiety.

    Time frame: up to six months

  2. postoperative mobility

    The effects of routine patient education and video-assisted mobilization training on postoperative mobility in patients undergoing coronary artery bypass graft surgery were investigated. Patient Mobility Scale and Observer Mobility were used to measure the level of postoperative mobility. The patient mobility and observer mobility scale consists of two parts: "Patient Mobility" and "Observer Mobility". The Patient Mobility Scale includes questions to measure the difficulty and pain experienced by the individual during activities such as turning from one side to the other in bed, sitting on the edge of the bed, standing up on the edge of the bed and walking in the patient room. It was evaluated using a 15 cm visual analog and verbal statements were included at the bottom. The Observer Mobility Scale consists of the assessment of 4 postoperative activities including turning, sitting, standing and walking. The patient's dependence or independence on the nurse is calculated.

    Time frame: up to six months

  3. postoperative pain

    The effects of routine patient education and video-assisted mobilization training on postoperative mobility in patients undergoing coronary artery bypass graft surgery were investigated. Patient Mobility Scale and Observer Mobility were used to measure the level of postoperative mobility. The patient mobility and observer mobility scale consists of two parts: "Patient Mobility" and "Observer Mobility". The Patient Mobility Scale includes questions to measure the difficulty and pain experienced by the individual during activities such as turning from one side to the other in bed, sitting on the edge of the bed, standing up on the edge of the bed and walking in the patient room. It was evaluated using a 15 cm visual analog and verbal statements were included at the bottom. The Observer Mobility Scale consists of the assessment of 4 postoperative activities including turning, sitting, standing and walking. The patient's dependence or independence on the nurse is calculated.

    Time frame: up to six months

07

Study locations

1 site
  • Merve Tosun
    Tekirdağ, Teki̇rdağ 59700, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 3, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06117033
Lead sponsor
Namik Kemal University
Responsible party
Merve Tosun (Nurse, Namik Kemal University) — Principal investigator
First posted
Nov 3, 2023
Start date
Mar 15, 2023
Primary completion
Sep 15, 2023
Completion
Sep 15, 2023
Last update
Nov 3, 2023

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion