Effects of foot reflexology and therapeutic touch on women's health during hemodialysis
The Effect of Foot Reflexology and Therapeutic Touch on Fatigue, Depression and Quality of Sexual Life in Women Receiving Hemodialysis Treatment
This study tests whether foot reflexology and therapeutic touch can help women on hemodialysis feel less tired, less depressed, and improve their sexual quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 99 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Osmaniye Korkut Ata University Academic / other |
| Locations | 1 site (Osmaniye) |
| Trial ID | NCT06411652 on ClinicalTrials.gov |
What this trial studies
This study examines how foot reflexology and therapeutic touch can impact fatigue, depression, and sexual quality of life in women undergoing hemodialysis. It addresses the unique challenges faced by female patients with chronic kidney disease, particularly the emotional and social burdens that can arise from treatment. By exploring these alternative therapies, the study aims to provide insights into improving the overall well-being of these women. The methodology involves assessing the psychological and sexual health outcomes of participants receiving these interventions.
Who should consider this trial
Good fit: Ideal candidates for this study are sexually active women aged between 18 and 65 who are receiving hemodialysis treatment.
Not a fit: Patients who are not sexually active or those with communication problems may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the quality of life for women undergoing hemodialysis by alleviating symptoms of fatigue and depression while improving sexual health.
How similar studies have performed: While the specific combination of therapies in this study may be novel, similar studies have shown positive outcomes with reflexology and therapeutic touch in improving quality of life in various patient populations.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Being sexually active * Volunteering to participate in the research Exclusion Criteria: * The patient is 65 years or older or under 18 years of age * Having a communication problem
Where this trial is running
Osmaniye
- Osmaniye New State Hospital — Osmaniye, Turkey (Recruiting)
Study contacts
- Study coordinator: Cansu AĞRALI
- Email: agralicansu9@gmail.com
- Phone: 05317461333
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.