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The Effect of Education Hemodialysis Patients According to Roy Adaptation Model

The Effect of Education on Fluid Management, Symptom Control and Quality of Life ın Hemodialysis Patients According to Roy Adaptation Model

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05187234
Enrollment
107
Registered
2022-01-11
Start date
2019-12-09
Completion date
2020-12-12
Last updated
2022-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodialysis

Keywords

fluid management,symptom control,life quality

Brief summary

The study was conducted in order to evaluate the effect of the training provided to hemodialysis patients according to Roy Adaptation Model on fluid management, symptom control, and quality of life. The study was carried out as a randomized controlled trial with the participation of 107 patients (53 experimental, 54 control) The patients in the experimental group were provided with training based on Roy Adaptation Model, and training booklets were handed out.The control group did not attempt any intervention.

Detailed description

The most difficult domain for hemodialysis patients is fluid-salt restriction. Patients with inadequate fluid compliance/adherence experience many symptoms that negatively affect their life. The study was carried out as a randomized controlled trial with the participation of 107 patients (53 experimental, 54 control). The data were collected by using Patient Information From, Fluid Control in Hemodialysis Patients Scale (FCHPS), Dialysis Symptom Index (DSI), and Nottingham Health Profile (NHP). The forms were filled out by having interviews with the patients in the experimental and control groups in the 0th, 1st, and 3rd months. The patients in the experimental group were provided with training based (face to face individual) on Roy Adaptation Model (0th(onset)and 1st month), and training booklets were handed out. The Training was about 30-45 minutes. control group did not attempt any intervention. Routine maintenance of the control and experimental group and continued. When comparing the experimental and control groups, onset 0th month, 1st month and 3rd month measurements were taken into consideration. All scales were administered to the experimental and control groups at month 0 (onset), 1 and 3 months. The data were analyzed by using descriptive statistics methods with NCSS (Number Cruncher Statistical System) 2007 software, Student's t-test, Mann-Whitney U Test, Pearson Chi-square test, Fisher-Freeman-Halton Exact test, Repeated Measures test, Bonferroni testi Significance was accepted as p\<0,05.

Interventions

OTHEREducation

Experimental: intervention group Education and training booklet based on the Roy adaptation model was given to the patients. The training was repeated at the first welcome and after the first month.

Sponsors

Kırklareli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients with end-stage chronic kidney disease older than 18 years undergoing routine hemodialysis treatment for at least 3 months having 3 hemodialysis sessions literate volunteered to participate in the study

Exclusion criteria

Patients with acute renal failure previously diagnosed with liver failure and/or malignancy ,patients with New York Heart Society class 3-4 heart failure a history of kidney transplantation

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline fluid controlAt the end of the 1.st and 3 rd monthEvaluated by Fluid Control Scale in Hemodialysis Patients. the scale. The lowest score obtained from the scale was 24 and the highest score was 72, and the higher the score, the greater the compliance of the patients with fluid control.
Change from baseline in symptom severity in patientsAt the end of the 1.st and 3 rd monthEvaluated by 'Dialysis Symptom Index' Using this scoring system, the minimum possible total severity score was 0 if none of the 30 symptoms was present and the maximum potential. Score was 150 if all of the 30 symptoms were reported and rated as very much bothersome. The minimum value is 0 and the maximum value is 150.
change from baseline quality of life in patientsAt the end of the 1.st and 3 rd monthEvaluated by' Nottingham Health Profile'. It includes 38 items divided into six categories: sleep, physical mobility, energy, pain, emotional reactions, and social isolation. for each of the sections range between 0 ('worst health') and 100 ('best health').

Secondary

MeasureTime frameDescription
change from baseline ıntradialytic Weight GainAt the end of the 1.st and 3 rd monthInterdialytic weight gain was defined as the difference between the predialytic weight and weight at the end of the previous dialysis session

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026