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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05473845
Other study ID # HUTLI
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 11, 2022
Est. completion date July 21, 2022

Study information

Verified date July 2022
Source Mardin Artuklu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research was conducted with the aim of determining the effect of levels of pain and fatigue of acupressure and Reiki application on cancer patients receiving palliative care. The research was a single-blind, repeated measures, randomized controlled study. Research data were collected between February and July 2022. The research sample consisted of acupressure and Reiki application groups and a control group with 52 patients in each group, a total of 156 patients. Data was collected by means of a Patient Description Form, an Analgesic Follow-up Form, the Eastern Cooperative Oncology Group Performance Status Scale, the Numeric Pain Rating Scale, and the Brief Fatigue Inventory.


Recruitment information / eligibility

Status Completed
Enrollment 156
Est. completion date July 21, 2022
Est. primary completion date July 21, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. having a diagnosis of third or fourth-stage cancer, 2. being aged 18 years or older, 3. having had pain for at least one month in connection with cancer treatment or the symptoms of the disease, 4. using NSAII or non-opioid analgesics, 5. having a status of 3 or more on the Numeric Pain Rating Scale (NPRS), 6. having a score of 0-3 on the ECOG-PS scale Exclusion Criteria: 1. having a diagnosis of first or second-stage cancer, 2. being aged less than 18 years, 3. having bone or brain metastasis, 4. using opioid analgesics, 5. having a status of less than 3 on the NPRS, 6. having a status of between 4 and 5 on the ECOG-PS scale

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupressure intervention
Acupressure
Reiki intervention
Reiki

Locations

Country Name City State
Turkey Hediye Utli Mardin

Sponsors (1)

Lead Sponsor Collaborator
Mardin Artuklu University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numeric Pain Rating Scale A score of 0 indicates no pain, 1-3 slight pain, 4-6 moderate pain, and 7-10 severe pain . on the second day of the starting week
Primary Brief Fatigue Inventory It is scored between 0 and 10. on the second day of the starting week
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