- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07357194
Renal Rehabilitation Among Patients With Kidney Failure
Barriers to Renal Rehabilitation Among Patients With Kidney Failure in Governmental Hospitals in Cairo: A Cross-Sectional Study
Study Overview
Status
Conditions
Detailed Description
This study is a cross-sectional design aimed at identifying the barriers to renal rehabilitation among patients diagnosed with kidney failure in governemtnal hospitals in Cairo.
The sample size for this study was determined using G*POWER statistical software (version 3.1.9.2; Franz Faul, Universitat Kiel, Germany) and was based on a previous study by (Bossola et al., 2014). which reported a prevalence of 38.1%. The required sample size calculated for this study is N=155, with calculations made using a significance level (α) of 0.05 and a statistical power of 80%. This sample size is deemed appropriate for achieving the study's objectives and ensuring statistically significant results.
155 patients suffering from kidney failure will participate in the study. They will be selected randomly from the different governmental hospitals centers in Cairo, Informed consent Freely and voluntarily consent to participate in this research study (Effect of pelvic floor down-training exercise on females with idiopathic overactive bladder) under the supervision and direction of the researcher/ Merna Mabrouk A thorough description of the study procedures has been explained to me, and I understand that I may withdraw my consent and discontinue participation in this study research at any time without prejudice to me.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Giza Governorate
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Giza, Giza Governorate, Egypt, 3387722
- Faculty of Physical Therapy
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
- Participants must have a confirmed diagnosis of kidney failure,
- Participants must be 18 years of age or older
- Participants must be willing and able to provide written informed consent (Appendix I).
- Participants must be receiving treatment at one of the nephrology clinics in Cairo that are involved in the study.
Severe Cognitive Impairment or Psychiatric Disorders
- Recent Participation in Similar Studies
- Acute Medical Condition
- Inability to Communicate
- Pregnancy
- Non-residency in Cairo
- Non-compliance with Treatment
Description
Inclusion Criteria:
Participants must have a confirmed diagnosis of kidney failure,
- Participants must be 18 years of age or older
- Participants must be willing and able to provide written informed consent (Appendix I).
- Participants must be receiving treatment at one of the nephrology clinics in Cairo that are involved in the study.
Exclusion Criteria:
Severe Cognitive Impairment or Psychiatric Disorders
- Recent Participation in Similar Studies
- Acute Medical Condition
- Inability to Communicate
- Pregnancy
- Non-residency in Cairo
- Non-compliance with Treatment
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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1
Patients with kidney failure doing dialysis
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Dialysis patients' perception regarding exercise benefits and barriers Questionnaire (DPEBBS)
Time Frame: 20 minutes
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The perception of dialysis patients regarding exercise benefits and barriers will be measured using the DPEBBS
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20 minutes
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Under request from Cairo Unive
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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