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.

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