Quality of Life, Anxiety and Fatigue Level of Parkison's Patients With Color Therapy

Sponsor
Ataturk University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06154772
Collaborator
(none)
60
1
2
7
8.6

Study Details

Study Description

Brief Summary

The aim of this study was to investigate the effect of color therapy on quality of life, anxiety and fatigue levels in patients with Parkinson's disease.

Condition or Disease Intervention/Treatment Phase
  • Other: Color Therapy
N/A

Detailed Description

Color Therapy aims to balance and heal our body's energy centers using the seven color spectrum, which helps to promote our body's own healing process. Thus good health and well-being is achieved through the balance of all these energies. Color therapy basically consists of color and character analysis with name, color therapy with chakras, programming of the pendulum, chakras and color application, color application with water, color application with colored light device.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study is an experimental study with pre-test and post-test control groupsThis study is an experimental study with pre-test and post-test control groups
Masking:
Single (Participant)
Masking Description:
Single
Primary Purpose:
Supportive Care
Official Title:
The Effect of Color Therapy on Quality of Life, Anxiety and Fatigue Levels of Parkison Patients
Anticipated Study Start Date :
Nov 27, 2023
Anticipated Primary Completion Date :
Apr 27, 2024
Anticipated Study Completion Date :
Jun 27, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Color Therapy

Balancing body chakras with colors. Colors are applied to the body's chakras for 10-15 minutes.

Other: Color Therapy
Color therapy will be applied to the body chakras for 10-15 minutes with colored fabrics, color therapy with water and colored light lamp.

No Intervention: Control Group

Routine maintenance will be applied

Outcome Measures

Primary Outcome Measures

  1. Quality of Life Scale (SF36) [At the end of Color Therapy (therapy 9 times in total in 3 months)]

    It was developed to measure the quality of life in people with physical diseases. It is measured in 8 dimensions and 36 items: physical function, physical role difficulty, emotional role difficulty, viability, mental health, social functionality, pain, and general health perception.

  2. Beck Anxiety Inventory (BAI) [At the end of Color Therapy (therapy 9 times in total in 3 months)]

    It consists of 21 questions and a minimum score of 0 and a maximum score of 3 is obtained from each question. As a result of the answers to all questions, all answers are summed up and a total score is obtained. In the evaluation phase, the presence and level of depression is interpreted in line with the meanings expressed by the score ranges. In the evaluation, 0-9 point range defines the presence of minimal depressive symptoms, 10-16 point range defines the presence of mild depressive symptoms, 17-29 point range defines the presence of moderate depressive symptoms and 30-63 point range defines the presence of severe depressive symptoms. A score of 17 and above indicates a level of depression that may require treatment.

  3. Parkinson's Fatigue Scale (PYO-16) [At the end of Color Therapy (therapy 9 times in total in 3 months)]

    It consists of 16 items, with 5 responses for each item (1=strongly disagree, 5=strongly agree). The result evaluation can be done in two different ways. The total value is calculated as the average of the response to all items (value range 1-5). Scores above the average "3.3" are considered tired. In the other rating option, 0 (actual response 1-3) and 1 (actual response 4-5) are scored, with a total value between 0-16. A total of 8 points and above is considered tired. In both methods, a higher value indicates a higher level of fatigue.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Having been diagnosed with Parkinson's disease for at least 6 months,

  • Those who have not taken sleeping pills or sedative drugs,

  • Not having undergone brain stimulation surgery,

  • Do not have a physical illness or cognitive disability that would prevent them from understanding the education provided, and do not have a diagnosis of a psychiatric disease,

  • According to the Parkinson's Fatigue Scale, the scale score is >8

  • The patient or someone living in the same house with the patient is literate,

  • Patients have no vision problems.

Exclusion Criteria:
  • Parkinson patients who did not agree to participate in the research

Contacts and Locations

Locations

Site City State Country Postal Code
1 Firat University Elazıg Turkey

Sponsors and Collaborators

  • Ataturk University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
gülcan bahcecioğlu, Principal Investigator, Ataturk University
ClinicalTrials.gov Identifier:
NCT06154772
Other Study ID Numbers:
  • 27/09/2023
First Posted:
Dec 4, 2023
Last Update Posted:
Dec 4, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by gülcan bahcecioğlu, Principal Investigator, Ataturk University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 4, 2023