- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05208073
Effectiveness of Cosmetic Therapy on Self-esteem and Depression for Elderly Residents in Long-Term Care Institutions
March 21, 2022 updated by: Tsui-Wei Chien, National Taipei University of Nursing and Health Sciences
Cosmetic therapy provides a psychological effect on the elderly, improving their self-confidence and social participation.
This study was conducted to investigate the effectiveness of cosmetic therapy to enhance the self-esteem and reduce depression of elderly residents in long-term care institutions.
We expect that a 6-week cosmetic therapy will improve the elderly's mental health, including depression and self-esteem.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan
- Yi-xing Elderly long-term care center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years to 100 years (OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Aged over 65 years old.
- Having been admitted to a long-term care institution (conservation type) for three months.
- Be able to communicate in Mandarin, Taiwanese and written languages.
- The total score of Mini-mental state examination (MMSE) is higher than 24 points.
- The muscle strength of the left or right hand is 4 points (inclusive) or above, and the maintenance and makeup procedures can be operated with one or both hands.
- After the researcher's explanation, the participant is willing and able to give informed consent for participation in the study.
Exclusion Criteria:
- Under the age of 65.
- The applicant has been admitted to a long-term care institution (conservation type) for less than three months.
- Unable to communicate in Mandarin, Taiwanese and written language.
- Participated in cosmetic therapy.
- Diagnosed with mental illness (except depression), dementia and delirium.
- Currently taking antidepressant drugs.
- Currently receiving depression-related treatment.
- The maintenance and makeup steps cannot be operated with assistance.
- Failure to sign the research consent form.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Intervention group
The experimental group received 6-week cosmetic therapy.
|
The cosmetic therapy in this study is once a week, 60 minutes each section for a total of 6-week.
Cosmetic therapy uses the teaching materials to teach the subjects skincare and makeup operation steps and use the 10-minute limb stretching to relax their minds before the activity, and then lead the research subjects to use cotton pads to apply lotion and lotion.
, female subjects used powder, eyebrow pencil, and lipstick (or lip balm) to complete weekly different-themed activities and hairstyling, while men performed weekly different theme activities and hairstyling.
|
|
NO_INTERVENTION: Control group
The control group maintains the institution's original daily routine care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Geriatric Depression Scale short-form (GDS-SF)
Time Frame: Pre-test before cosmetic therapy intervention and post-test at the end of six-week cosmetic therapy
|
Geriatric Depression Scale short-form is a 15-item scale; each item on this scale uses a " Yes/ NO" answer method, and the scoring method is 1 point and 0 points.
The total score ranges from 0 to 15, with less than 5 indicating no depression symptoms, 5 to 9 indicating mild depression, greater than or equal to 10 indicating moderate to severe depression.
|
Pre-test before cosmetic therapy intervention and post-test at the end of six-week cosmetic therapy
|
|
Rosenberg Self-Esteem Scale (Chinese version)
Time Frame: Pre-test before cosmetic therapy intervention and post-test at the end of six-week cosmetic therapy
|
Rosenberg Self-Esteem Scale (Chinese version) is a 10-item scale that measures the respondent's self-esteem.
Each item is scored on a 4-point Likert scale, ranging from 1 (strongly disagree) to 4 (strongly agree); the minimum and maximum scores on the scale are 10 and 40, with lower scores suggesting better self-esteem.
|
Pre-test before cosmetic therapy intervention and post-test at the end of six-week cosmetic therapy
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Tsui-Wei Chien, PhD, National Taipei University of Nursing and Health Sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
December 1, 2021
Primary Completion (ACTUAL)
February 14, 2022
Study Completion (ACTUAL)
February 28, 2022
Study Registration Dates
First Submitted
January 12, 2022
First Submitted That Met QC Criteria
January 12, 2022
First Posted (ACTUAL)
January 26, 2022
Study Record Updates
Last Update Posted (ACTUAL)
March 23, 2022
Last Update Submitted That Met QC Criteria
March 21, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- C110043
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
Clinical Trials on Aged
-
Federal University of Rio Grande do SulNot yet recruiting
-
Instituto Politécnico de BragançaUniversity of Alcala; Research Center for Active Living and WellbeingCompletedAged Healthy Volunteer | Aged 60 Years or OlderPortugal
-
Samsung ElectronicsCompletedAged | Adults | Middle Age | Aged, 80 and OverKorea, Republic of
-
Consorci Sanitari de l'Alt Penedès i GarrafCompletedAged | Patient Safety | Aged, 80 and Over | Restraint, PhysicalSpain
-
Gulf Medical UniversityRecruitingAged | Geriatric | Balance | Fall Risk, Fall Prevention | Aged Healthy VolunteerUnited Arab Emirates
-
The Hong Kong Polytechnic UniversityThe University of Hong Kong; Education University of Hong KongRecruiting
-
University Hospital, ToulouseCompleted
-
Abbott NutritionCompleted
Clinical Trials on Cosmetic therapy
-
Unilever R&DMS Clinical Research Pvt. LtdNot yet recruiting
-
Pierre Fabre Dermo CosmetiqueCompleted
-
SVR GroupCompletedAtopic DermatitisBelgium
-
Superior UniversityCompletedCosmetic Product Causing Toxic EffectPakistan
-
Johnson & Johnson Consumer Inc. (J&JCI)University of SheffieldTerminated
-
Pierre Fabre Dermo CosmetiqueCompleted
-
Federico II UniversityCompleted
-
Medical University of WarsawCompletedTelogen Effluvium | Androgenetic Alopecia (AGA) | Female Pattern Hair Loss, Androgenic Alopecia
-
Johnson & Johnson Vision Care, Inc.CompletedVisual AcuityUnited States, Hong Kong
-
Amazentis SAproDERM GmbHCompleted