Evaluation of the Effect of the Training Program Based on the Precede-Proceed Model on Guality Life Style

Sponsor
Ataturk University (Other)
Overall Status
Completed
CT.gov ID
NCT05955703
Collaborator
(none)
72
1
2
13.7
5.3

Study Details

Study Description

Brief Summary

This study was conducted to evaluate the effect of a Precede-Proceed Model-based (PPM-based) training program on treatment adherence, healthy lifestyle behaviors, and quality of life of hemodialysis patients.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: ppm based training
N/A

Detailed Description

The Precede proceed model includes structured training phases to bring positive behavior change. The model, which consists of training phases, provides the researcher with the opportunity to identify the problem and the deficiencies that cause the problem, evaluate the quality of life with these deficiencies and develop a health program for its solution. In order to apply the nine-phase model, the individual-patient's voluntary cooperation, determination and active participation in health practices are required.

Study Design

Study Type:
Interventional
Actual Enrollment :
72 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Evaluation of the Effect of the Training Program Based on the Precede-Proceed Model on Adherence to Treatment and Healthy Lifestyle Behaviors of Hemodialysis Patients
Actual Study Start Date :
Oct 18, 2021
Actual Primary Completion Date :
Dec 8, 2022
Actual Study Completion Date :
Dec 8, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Using the experimental group as a result of the training based on PPM

The training sessions planned within the scope of PPM were applied to the patients, who were divided into groups of six according to the bed order, for 15-20 minutes for eight weeks, when the patients felt well, through training booklets and power point presentations. When the trainings started, the posters prepared were hung in the waiting room while the intervention group was undergoing hemodialysis. The person providing the care of the patient was included in each training. During the trainings, it was requested that the training booklets be with the patients and the power point presentations continued in parallel with the training booklets. Post-test was applied to intervention group three months after the post-test application, follow-up test was applied to the intervention group in order to evaluate the impact.

Behavioral: ppm based training
The training program based on the precede proceed model was applied to hemodialysis patients for 8 sessions. Eight sessions of training were given to the experimental group within the scope of the model, a booklet was developed in line with the trainings and posters were prepared.

No Intervention: Using the control group as a result of the training based on PPM

After the follow-up test, training was given to the patients in the control group and a model-based training booklet was distributed.

Outcome Measures

Primary Outcome Measures

  1. Evaluation of the Effect of the Training Program based on the Precede-Proceed Model on quality of life style of Hemodialysis Patients [six month]

    The patients' quality of life was evaluated with the SF-12 Quality of Life scale. The scale consists of 12 items. There is no breakpoint. The higher the score obtained from the scale, the higher the quality of life.

Secondary Outcome Measures

  1. 2. Evaluation of the Effects of the Continuation Test (follow-up test results 3 months after the post-test) and the Education Program Based on the Pre-Continuation Model on the Quality of Life of Hemodialysis Patients [three month]

    The patients' quality of life was evaluated with the SF-12 Quality of Life scale. The scale consists of 12 items. There is no breakpoint. The higher the score obtained from the scale, the higher the quality of life.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18 years of age or older,

  • Hemodialysis treatment for at least 6 months,

  • A total score of 1 or more from the Dialysis Diet and Fluid Restriction Non-Compliance Scale,

  • A score between 1 and 7 on the scale of compliance with medical treatment,

  • Place, time, person orientation,

  • Does not have a psychiatric illness or a problem that prevents written or verbal communication,

Exclusion Criteria:
  • Diagnosed with psychiatric illness Individuals with a diagnosis of malignancy wanting to leave research

  • Those who do not attend all of the trainings / do not want to continue

  • Individuals whose general condition is deteriorated

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ataturk University Erzurum Yakutiye Turkey

Sponsors and Collaborators

  • Ataturk University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ayşenur SARIASLAN, Assist. Prof., Ataturk University
ClinicalTrials.gov Identifier:
NCT05955703
Other Study ID Numbers:
  • AYSENUR-TEZ
First Posted:
Jul 21, 2023
Last Update Posted:
Jul 21, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ayşenur SARIASLAN, Assist. Prof., Ataturk University

Study Results

No Results Posted as of Jul 21, 2023