search
Back to results

Longitudinal Trial Assessing Cellulite in Women Wearing a New Compression Garment

Primary Purpose

Cellulite

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Compression garment with Vari-pad microdots ink-printed on inside.
Sponsored by
The Whiteley Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cellulite focused on measuring compression

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Biological females, over the age of 18 years old, who are able to walk normally and who have cellulite on their buttocks and/or upper thighs. Due to having to produce special garments for this trial where only half of the garment has the Vari-pads, there will be for following restrictions: Total number = 60. Volunteers will be asked their sizes (Small, Medium, Large and Extra large) and will only be invited to attend if there are available places in that category. Sizes: Small = 10 Medium = 20 Large = 20 Extra large = 10 Exclusion Criteria: Women under 18 years of age. Women who are pregnant or who intend to get pregnant in the next 6 months. Women with no discernible cellulite on initial examination. Women undergoing any other treatment which aims to reduce the appearance of cellulite. Women who are unable to complete at least 3 months of this trial.

Sites / Locations

  • The Whiteley ClinicRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Study Cohort

Arm Description

A cohort of 60 biological females who volunteered to be part of the 6 months study.

Outcomes

Primary Outcome Measures

Time to subjective improvement on side with Vari-pads
Time to notice difference in cellulite between the sides when wearing garment with one side having Vari-pads.

Secondary Outcome Measures

Quality of life changes
Quality of life changes by Celluqol® questionnaire at 0, 3 and 6 months. The Celluqol tool gives a numerical outcome 8-40: From 8 to 16 points - cellulite does not affect quality of life From 16 to 24 points - cellulite slightly affects quality of life From 24 to 32 points - cellulite reasonably affects quality of life From 32 to 40 points - cellulite intensely affects quality of life
Objective clinical assessement of photographs by 2 blinded observers
Changes in photographs 0,3,6 months as assessed by 2 blinded observers who are clinicans expereinced in cellulite assessment. Each photograph will be blinded by a numerical code and blinded assessment will be by scoring 0-10. 0 is the worst posisble cellulite and 10 being no cellulite visible at all.
Transcutaneous water content
Changes in transcutaneous water measurements - this is a numerical meaurement direct from the device.

Full Information

First Posted
June 28, 2023
Last Updated
July 24, 2023
Sponsor
The Whiteley Clinic
search

1. Study Identification

Unique Protocol Identification Number
NCT05959681
Brief Title
Longitudinal Trial Assessing Cellulite in Women Wearing a New Compression Garment
Official Title
Longitudinal Trial Assessing Cellulite in Women Wearing a New Compression Garment - One Side With Ink Printed Micro-pads ("Vari-pads") and One Side Without.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2023 (Anticipated)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
April 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Whiteley Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators are investigating a compression garment that appears to reduce the appearance of Cellulite. The garment has both compression and patented ink-printed micro-dots ("Vari-pads"). These Vari-pads on the inner aspect of the garment are thought to increase the lymphatic return over compression alone. In this study, volunteers with cellulite are asked to wear the garment, with only one side (left or right) having the active Vari-pads. The participants wear the garment for at least 8 hours per day. If, and when, the participants notice a difference between the sides (left and right sides), the participants will notify the investigators. At this point the participants will be invited to the trial centre for an assessment and to be swapped to a garment with Vari-pads on both sides. Apart from this variable end-point, the participants will be reviewed routinely at 3 and 6 months. The trial ends at 6 months.
Detailed Description
The product being tested is to be a retail (non-medical) garment. This garment is a pair of standard compression shorts with a pattern of small, raised pads ("Vari-pads") of different heights printed on the inner aspect. A previous trial has suggested that wearing this garment for over eight hours a day can reduce the appearance of cellulite. In addition, participants found these compression pants to be very comfortable. In this proposed trial, the investigators wish to investigate whether the previously found subjective and objective improvement of the appearance of cellulite is due to the compression alone, or whether the Vari-pads on the inside of the product enhance the subjective or objective impression of cellulite. As such, the investigators have asked the manufacturer to produce 60 pairs of pants where the Vari-pads are printed onto the inner aspects as per usual on one side, but not on the other side. On this other side, there will be a dot of the same colour printed, but it will not be raised. The participants will be asked to wear the apparel for eight hours or more a day, at times that the participants find most suitable. If and when the participants notice a difference in the appearance of cellulite between the right and left side, the participants will notify the investigators. At this point the investigators will invite the participants to the trial centre for an assessment. The participants will be swapped into the normal garments which have Vari-pads on both sides. The participants will then wear these garments for the remainder of the trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cellulite
Keywords
compression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective observational cohort study.
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Study Cohort
Arm Type
Experimental
Arm Description
A cohort of 60 biological females who volunteered to be part of the 6 months study.
Intervention Type
Device
Intervention Name(s)
Compression garment with Vari-pad microdots ink-printed on inside.
Intervention Description
Initially, participants wear a garment with Vari-pads on one side (left or right) only and swap to a garment with Vari-pads on both sides if / when the participants notice a difference between the sides. Wearing garment 8 hours per 24 hours.
Primary Outcome Measure Information:
Title
Time to subjective improvement on side with Vari-pads
Description
Time to notice difference in cellulite between the sides when wearing garment with one side having Vari-pads.
Time Frame
0-6 months
Secondary Outcome Measure Information:
Title
Quality of life changes
Description
Quality of life changes by Celluqol® questionnaire at 0, 3 and 6 months. The Celluqol tool gives a numerical outcome 8-40: From 8 to 16 points - cellulite does not affect quality of life From 16 to 24 points - cellulite slightly affects quality of life From 24 to 32 points - cellulite reasonably affects quality of life From 32 to 40 points - cellulite intensely affects quality of life
Time Frame
0-6 months
Title
Objective clinical assessement of photographs by 2 blinded observers
Description
Changes in photographs 0,3,6 months as assessed by 2 blinded observers who are clinicans expereinced in cellulite assessment. Each photograph will be blinded by a numerical code and blinded assessment will be by scoring 0-10. 0 is the worst posisble cellulite and 10 being no cellulite visible at all.
Time Frame
0-6 months
Title
Transcutaneous water content
Description
Changes in transcutaneous water measurements - this is a numerical meaurement direct from the device.
Time Frame
0-6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Biological females, over the age of 18 years old, who are able to walk normally and who have cellulite on their buttocks and/or upper thighs. Due to having to produce special garments for this trial where only half of the garment has the Vari-pads, there will be for following restrictions: Total number = 60. Volunteers will be asked their sizes (Small, Medium, Large and Extra large) and will only be invited to attend if there are available places in that category. Sizes: Small = 10 Medium = 20 Large = 20 Extra large = 10 Exclusion Criteria: Women under 18 years of age. Women who are pregnant or who intend to get pregnant in the next 6 months. Women with no discernible cellulite on initial examination. Women undergoing any other treatment which aims to reduce the appearance of cellulite. Women who are unable to complete at least 3 months of this trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mark S Whiteley, MS FRCS MBBS
Phone
03300581850
Email
mark@thewhiteleyclinic.co.uk
Facility Information:
Facility Name
The Whiteley Clinic
City
Guildford
ZIP/Postal Code
GU2 7RF
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark S Whiteley, MS FRCS MBBS
Phone
0330 0581 850
Email
mark@thewhiteleyclinic.co.uk

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35104044
Citation
Arora G, Patil A, Hooshanginezhad Z, Fritz K, Salavastru C, Kassir M, Goldman MP, Gold MH, Adatto M, Grabbe S, Goldust M. Cellulite: Presentation and management. J Cosmet Dermatol. 2022 Apr;21(4):1393-1401. doi: 10.1111/jocd.14815. Epub 2022 Feb 14.
Results Reference
background
PubMed Identifier
37750084
Citation
Kiely MJ, Poulsen A, Muschamp SD, Sallis C, Whiteley MS. Participant Reported Improvement in Cellulite by Vari-Pad Apparel and Objective Measurements - A "First Use" Pilot Study. Clin Cosmet Investig Dermatol. 2023 Sep 20;16:2573-2583. doi: 10.2147/CCID.S426978. eCollection 2023.
Results Reference
background
PubMed Identifier
632386
Citation
Nurnberger F, Muller G. So-called cellulite: an invented disease. J Dermatol Surg Oncol. 1978 Mar;4(3):221-9. doi: 10.1111/j.1524-4725.1978.tb00416.x.
Results Reference
background
Citation
Hexsel D, Weber MB, Taborda ML, Dal'Forno T, do Prado DZ. Celluqol® - a quality of life measurement for patients with cellulite. Surgical and Cosmetic Dermatology 2011 (Jan);3(2):96-101
Results Reference
background

Learn more about this trial

Longitudinal Trial Assessing Cellulite in Women Wearing a New Compression Garment

We'll reach out to this number within 24 hrs