RESEARCH PARTICIPANT NEEDED FOR NEW STUDY

 

www.newstudy.info

 

 

Dear Participant,  

Please only send your reply to:  newstudy@sbcglobal.net

Stephens & Associates is a privately owned, worldwide research organization serving companies in North America, Europe, and Asia. We conduct clinical studies every week, and we have studies for male and female mostly age 18 and up.

1. To be consider for any study, please make sure to join our database first. Just click JOIN/ REGISTER.

2. Due to high volume of email/ call responses, If you reply, and do not hear back from us after 48 hours, please assume the study had been filled, and please check our web site regularly to apply for another study. We have new study listed almost everyday, and we sincerely appreciate your interest!
 

3. Please ALWAYS have the study number handy when you call, so we can go over the study quicker.

4. ANY "NO-SHOW" will not be considered for future studies. Please always call if you could not keep your appointment.

 

 

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Important Notes:  

 

1.  Please always read the schedule and detail of each study before you sign up.

2.  We are open for phone calls mostly between 10:00am-8:00pm.

3.  If you have small children, you can bring them with you to most studies.

4.  You can only do 1 face usage study at a time (4 weeks break between face usage study).

5.  Please keep checking the website directly, instead of waiting for the email. It will help you to get in a study quicker.

6.  Women who have had a baby within the past “3 months” will not be able to participate. Anyone who is pregnant or nursing will not qualify for these studies.

7.    We always send out the reminder email for everyone 1day before the study. Everyone needs to confirm their appointment once you get that email, either by phone or by email. If you do not confirm, your name might be replaced.

 

 

 

 

 

 

 

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CURRENT STUDIES:

Below is the full detail of all of the studies. We are extremely busy, so please help us to read over the detail and please ONLY call if you can fit the qualification and can SHOW UP. “No show” will NOT be considered for future studies.

 

We will expect to have lot of great studies coming up, so please make sure to check the website regularly or check our Facebook page, so you don't miss out!

 

African American Male and Female: please check out D028, D093.

 

LOT OF STUDY COMING UP FOR BABY PRODUCTS - WILL POST SOON.

 

MORE ACNE STUDY- WILL POST SOON. (If you do not qualify for an Acne study recently, you can always try again, as long as you fit the description).

 

 

 

 

General Rule - Break time in between 2 studies:

 

FYI- You must have 4 weeks break in between 2 facial studies. The Clinic will check your record every time, please keep track with the last date you had finished the last study.

 

 

4 week washout between 2 face studies.

2 week washout between a patch and a face.

 

 

 

 

 

 

1. D204- ULTRASOUND DEVICE STUDY

 

Thomas J. Stephens & Associates, Inc., a global research organization is seeking

 

MALES & FEMALES, AGES 35 - 60, WITH MILD TO MODERATE FACIAL SAGGING, LAXITY, AND SUPERFICIAL WRINKLES

 

To participate in our upcoming research study.

 

Study Objective:   This study is being conducted to determine both the impact of a maintenance regimen and if regression occurs after daily treatment (5 days per week for 5 weeks) with a handheld ultrasound device designed for facial rejuvenation.   

 

Eligibility:    Males & Females, ages 35 to 60, all skin types, with mild to moderate facial sagging, laxity and superficial wrinkles in the lower jaw/upper neck area.

 

Compensation:  Up to $1000.00

 

START:    4/17- anytime between 11:00am- 12:30pm.

END:        8/25 or 8/27  (38 Visits total)

 

 

Everyone will have their height and weight measured. Please know your weight before you call. Thank you!

 

For this study,  Everyone must START on 4/17, After the first 2 visits, Must go EVERYDAY From 4/23 until 5/23 (Monday thru Friday) .

 

Most of the Visits will be only 45 minutes, accept Assessment Visits will be longer. You will have some Assessment Visits combined with Treatment Visits on the same day.

 

For men: Must have No Facial hair.

 

 

 

Screening

Baseline

7 Assessment Visits

 

 

 

Some Assessment and Treatment Visits will fall in the same day.

 

 

 

25 Treatment Days*

T1: Treatment 1, etc...

Mon-Friday

 

All treatment days: Flexible schedule

Anytime 9:00-11:45am or 1:00-6:15pm

 

 

Visit 1

 

START 4/17/14

Anytime between 11:00am-12:30 pm.

 

(Visit will take 1hr)

 

 

 

Visit 2

04/18/14

 

All visits: flexible

 

9:00am – 12:00pm

OR

1:00pm to 3:00pm

 

 

Visit 3

04/23/14

 

9:00am-11:45am

or

1:00-6:15

 

Visit 8

04/30/14

9:00-11:45

or

1:00-6:15

 

Visit 13

 

05/07/14

9:00-11:45

or

1:00-6:15

 

Visit 18

05/14/14

9:00-11:45

or

1:00-6:15

 

Visit 23

05/21/14

9:00-11:45

or

1:00-6:15

Visit 28

05/29/14

9:00-11:45

or

1:00-6:15

 

Visit 38

08/27/14

9:00-11:45

or

1:00-6:15

 

 

T1-T5(Visit 3-Visit 7):

 

Must go everyday Monday - Friday

 

04/21/14 – 04/25/14

 

T6-T10(Visit 8-12):

 

Must go everyday

Monday - Friday

 

04/28/14 – 05/02/14

 

T11-T15(Visit 13-V17):

 

Must go Everyday Mon- Friday

 

05/05/14 – 05/09/14

 

T16-T20(Visit 18-V22):

 

Must go Everyday Mon- Friday

 

05/12/14 – 05/16/14

 

T21-T25(V23-V27):

05/19/14 – 05/23/14

 

 

Make-Up Treatments:

05/27/14 – 06/04/14

 

Visits 29-31: 

06/23/14

06/24/14

06/25/14

 

Visits 32-34:  07/21/14

07/22/14

07/23/14

 

Visits 35-37:  08/18/14

08/19/14

08/20/14

 

 

 

 

 

 

All interested panelists must be screened and scheduled by Joanne Luu.

For consideration, please call: 

 

 

Joanne Luu

972-716-0630

Email: Joanne@newstudy.info

www.newstudy.info

Facebook.com/Newstudy.info

 

Stephens And Associates (Global Research and Product Testing)

3310 Keller Springs Rd # 130

Carrollton, TX 75006

 

 

 

 

 

 

2. D093- FACE USAGE STUDY, OPEN FOR FEMALE AGE 35-65, (ASIAN, HISPANIC, CAUCASIAN, AFRICAN AMERICAN).  MUST HAVE NO FACE STUDY IN THE PAST 4 WEEKS.  MUST BE A REGULAR USER OF FACIAL MOISTURIZER.

 

MUST Avoid using shower oils, moisturizer, body lotion at least 3 days prior to visit 1.

 

START: SATURDAY 4/19

 

 

 

 

 

 

 

Visit: 1

Visit: 2

Visit: 3

Visit: 4

 

LAST GROUP !

19APR2014
Saturday
1:00 PM - 3:00 PM

03MAY2014
Saturday
1:00 PM - 2:30 PM

17MAY2014
Saturday
1:00 PM - 2:30 PM

31MAY2014
Saturday
1:00 PM - 2:00 PM

 

 

Anytime in between is ok.

Latest can be 3pm.

 

 

 

 

 

 

 

 

 

 

Number of Visit(s)

4

 

 

 

Compensation

$140.00 plus product

 

 

 

 

 

 

 

D093- QUALIFICATION:

Please answer the following questions below, then CALL Joanne asap to sign up (972-716-0630). These questions will be ask on Visit 1.

 

 

EXCLUSIVE: Subjects cannot participate on any other study.

 

MUST Remove all makeup at least 30 minutes prior to each scheduled clinic visit

 

 

 

 

   YES

 

      NO

 

1.

1. Do all of the following apply to you?

 

a)     Age – 35 to 65, Females Only

b)  80% of panel must be Asian, Caucasian, %10 Hispanic, 10% is African American.

c)     General Good Health - not taking lot of medication.

d)    Moderate crow’s feet wrinkles and skin imperfections.

e)  Regular user of facial moisturizing products.

f)      Healthy skin on face and forearms.

g)  BMI (body mass index) MUST BE LESS THAN  40.

h)     Had the following breaks from participating in clinical trials at Stephens or at another research facility or doctor’s office.

Ø  At least 4 weeks for face/usage study

Ø  At least 3 weeks for patch studies

 

 

 

2.

 

2. Do you have any of the following conditions? 

 

·         Disease or condition of the skin or eyes that would make it inappropriate for you to participate.

a)     Pregnant, nursing, or planning to become pregnant within the next six months, or have had a baby within the past 3 months.

b)    Uncontrolled metabolic diseases such as diabetes, hypertension, hyperthyroidism, or hypothyroidism.

c)     Severe psychological illness or intellectual inability to understand the study.

d)    Recent history of drug or alcohol abuse/addiction and/or study participation under the influence of alcohol and/or drugs.

e)  Permanent eye makeup (eyebrow and lid).

f)     Observable sunburn, suntan, scars, nevi, tattoo, excessive hair, scars, wounds, piercings, etc. or other dermal conditions on the face or arms.

g)    Pre-existing or dormant dermatologic conditions on the face or arms (e.g., psoriasis, neurodermatitis, rosacea, moderate to severe acne, moderate to severe active eczema, seborrheic dermatitis, severe excoriations etc.).

h)     History of immunosuppression/immune deficiency disorders (including HIV infection or AIDS).

i)      History of cancer in the past 10 years.

j)      Experienced illness with fever (above 101.3°F) lasting at least 24 hours within the last 7 days prior to the study start.

k)     Severe disease (severe heart/circulatory, liver, kidney or lung disease, severe diabetes mellitus) or chronic infections (hepatitis).

l)      Planned surgeries or invasive medical procedures during the course of the study.

m)   Diagnosed with known allergies to facial skin care products or cosmetic ingredients, prior intolerance responses after applying cosmetic products, or known sensitivities to AHA, BHA and/or PHA products, retinol products, moisturizers, or sunscreens.

 

 

 

3.

 

3. Had any of the following treatments/procedures, or are you currently taking or using any of the following medications?

a)     Anti-aging, anti-wrinkle, antioxidants treatments less than 30 days prior to the study entry.

b)    Ointments, creams, etc. for antibacterial, anti-allergic or immunosuppressive treatment of the skin on the face or forearms within the past 14 days or plan to during the study.

c)     Currently taking/have taken within the past 14 days certain medications or using topical products which in the opinion of the Investigator or designee may interfere with the study (e.g., prescription steroids and anti-inflammatory drugs, benzoyl peroxide, salicylic acid products, anti-wrinkle products, Q-10 moisturizers, etc., and any OTC skin treatment medications [including ointments, creams, etc. for antibacterial, anti-allergic or immunosuppressive treatment of the test sites]).

d)    Retin-A®, Retin-A Micro®, Renova®, Avita®, Tazorac®, Soriatane®, or Differin® within 4 months of the study start.

e)     Accutane® within 1 year of the study start.

f)   Antihistamines in the past 14 days or plan to during the study.

g)    Started hormone replacement therapies(HRT) or hormones for birth control less than 1 month prior to study start, or plan on starting, stopping, or changing their dosage or treatment modality during the study.

h)     Physical and/or cosmetic treatment at the test site(s) in the past 14 days or plan to during the study.

i)      Immunosuppressive medications (e.g., azathioprine, belimumab, cyclophosphamide, Enbrel, Imuran, Humira, mycophenolate mofetil, methotrexate, prednisone, Remicade, Stelara.) and/or radiation.

j)      Facial peel, photo facial, laser treatment, dermabrasion, Botox® injections, acid treatment, injectable filler treatment, facial plastic surgery or any other medical treatment administered  by a physician or skin care professional within the last 6 months which is designed to improve the appearance or firmness of facial skin.

 

 

 

4.

4. Do you understand and agree to follow these instructions?

a)     Avoid using skin care products as well as special skin care cleansing products such as shower oils at least 3 days prior to visit 1 and during the study.

b)    Avoid visits to saunas, swimming pools, and intensive sports at least 1 day prior to each scheduled visit.

c)     Avoid smoking at least 2 hours prior to each scheduled clinic visit.

d)    Remove all makeup at least 30 minutes prior to each scheduled clinic visit.

 

 

 

 

 

3. D082-EYE CREAM STUDY, OPEN FOR FEMALE (CAUCASIAN ONLY) AGE 35-60. MUST NOT BE IN ANY FACE STUDY PAST 4 WEEKS, OR PATCH STUDY PAST 3 WEEKS. VERY EASY STUDY! MUST BE A REGULAR USER OF A "LIQUID" FOUNDATION OR any facial product that has color to it. (concealer, spot treatment, etc...)

 

MUST NOT CURRENTLY TAKING ANTI HISTAMINE.

 

 

 

 

 

 

Date(s) of Study

 

Visit: 1

Visit: 2

Visit: 3

Visit: 4

18APR2014
Friday
9:30 AM - 12:00 PM

Anytime between is ok. Last appt can be up to 12 noon

02MAY2014
Friday
8:00 AM - 10:30 AM

16MAY2014
Friday
8:00 AM - 9:30 AM

30MAY2014
Friday
8:00 AM - 9:00 AM

 

Number of Visit(s)

4

 

Length of Visits:

Visit 1: 1.5 hour

Visits 2 & 3:   1 Hour

Visit 4: 45 Minutes

 

Compensation

$140.00 plus Eye Cream- Lot of openings! - Quick Paid!

 

 

 

 

 

D082 - QUALIFICATION:

Please answer the following questions below, then CALL Joanne asap to sign up (972-716-0630). These questions will be ask on Visit 1.

 

 

EXCLUSIVE: Subjects cannot participate on any other study.

 

MUST Remove all makeup.

 

 

 

   YES

 

      NO

 

1.

1. Do all of the following apply to you?

 

a)     Age – 35 to 60 - Caucasian Females Only

b)  Self-perceived normal, dry, combination, or oily facial skin.

c)     Moderate fine lines/wrinkles in the crow’s feet area.

d)    Moderate eye puffiness. (50% of panel, NOT everyone required.)

e)     Moderate dark circles. (50% of panel, NOT everyone required)

 

 Regular user of a tinted facial product. (Liquid Foundation, Concealer, Spot Treatment, BB Cream, etc.)

f)    Regular user of A a tinted product,( COULD BE a Moisturizer that has some color to it, or it can be a concealer, or spot treatment to cover blemishes, or a tinted primer, or anything that you use on your face that has a tinted / has some color to it, that will be ok).

 

 

g)    Had the following breaks from participating in clinical trials at Stephens or at another research facility or doctor’s office.

 

Ø  At least 4 weeks for face usages

Ø  At least 3 weeks for patch studies

 

 

 

 

 

2.

 

2. Do you have any of the following conditions?

 

a)     Disease or condition of the skin or eyes that would make it inappropriate for you to participate.

b)    Pregnant, nursing, or planning to become pregnant within the next six months, or have had a baby within the past 3 months.

c)     Uncontrolled metabolic diseases such as diabetes, hypertension, hyperthyroidism, or hypothyroidism.

d)    Diagnosed with known allergies to facial skin care products or cosmetic ingredients, prior intolerance responses after applying cosmetic products, or known sensitivities to AHA, BHA and/or PHA products, retinol products, moisturizers, or sunscreens.

e)     Pre-existing or dormant dermatologic conditions on the face or arms (e.g., psoriasis, neurodermatitis, rosacea, moderate to severe acne, moderate to severe active eczema, seborrheic dermatitis, severe excoriations etc.).

f)     Permanent eye makeup (eye brow and eyelid).

g)    Facial jewelry that cannot be removed.

h)     BMI > 40.

i)      History of cancer in the past 10 years.

j)      Experienced illness with fever (above 101.3°F) lasting at least 24 hours within the last 7 days prior to the study start.

k)     Planned surgeries or invasive medical procedures during the course of the study.

l)      Severe disease (severe heart/circulatory, liver, kidney or lung disease, severe diabetes mellitus) or chronic infections (hepatitis).

m)   History of immunosuppression/immune deficiency disorders (including HIV infection or AIDS).

n)     Recent history of drug or alcohol abuse/addiction.

o)    Observable sunburn, suntan, scars, nevi, tattoo, excessive hair, scars, wounds, piercings, etc. or other dermal conditions on the face or arms.

p)    Severe psychological illness or intellectual inability to understand the study.

 

 

 

3.

 

3. Had any of the following treatments/procedures, or are you currently taking or using any of the following medications?

 

a)     Routinely used any anti-aging, anti-wrinkle, antioxidants treatments less than 30 days prior to the study entry.

b)    Topical ointments, creams, etc for antibacterial, anti-allergic or immunosuppressive treatment of the skin on the face or forearms.

c)     Retin-A®, Retin-A Micro®, Renova®, Avita®, Tazorac®, Soriatane®, or Differin® within 4 months of the study start.

d)    Started hormone replacement therapies(HRT) or hormones for birth control less than 1 month prior to study start, or plan on starting, stopping, or changing their dosage or treatment modality during the study.

e) Currently taking antihistamines.

f)     Accutane® within 1 year of the study start.

g)    Immunosuppressive medications (e.g., azathioprine, belimumab, cyclophosphamide, Enbrel, Imuran, Humira, mycophenolate mofetil, methotrexate, prednisone, Remicade, Stelara.) and/or radiation.

h)     Prescription steroids and anti-inflammatory drugs, benzoyl peroxide, salicylic acid products, anti-wrinkle products, Q-10 moisturizers, etc., and any OTC skin treatment medications.

i)      Facial peel, photo facial, laser treatment, dermabrasion, Botox® injections, acid treatment, injectable filler treatment, facial plastic surgery or any other medical treatment administered  by a physician or skin care professional within the last 6 months which is designed to improve the appearance or firmness of facial skin.

 

 

 

 

 

 

 

 

 

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4. D028- Acne Study

 

 

 

SEEKING MALES & FEMALES, AGES 12 - 45, TO PARTICIPATE IN OUR UPCOMING CLINICAL RESEARCH STUDY

 

Study Objective:   This clinical trial is being conducted in order to assess the efficacy and tolerability of the Sponsor’s acne system compared to the efficacy and tolerance of a competitor’s acne system when used by males and females with mild to moderate acne vulgaris over the course of 8 weeks. 

 

Eligibility:    Males & Females, ages 12 to 45, all skin types, with mild to moderate facial acne. Prospective panelists must have between 10-50 inflammatory lesions and 10-100 non-inflammatory lesions to qualify.

 

Compensation:  Up to $225.00

Study Start Dates:  START 4/17

 

 

 

Visit: 1

Visit: 2

Visit: 3

Visit: 4

Visit: 5

 

 

 

Group: 9

17APR2014
Thursday
4:30 PM - 6:30 PM


Anytime in between is ok. Last appt can be up to 6:30pm.

01MAY2014
Thursday
4:30 PM - 6:30 PM

15MAY2014
Thursday
4:30 PM - 6:30 PM

29MAY2014
Thursday
4:30 PM - 6:30 PM

12JUN2014
Thursday
4:30 PM - 6:30 PM

 

 

 

 

All interested panelists must be screened and scheduled by Joanne Luu.

For consideration, please call: 

 

 

Joanne Luu

972-716-0630

Email: Joanne@newstudy.info

www.newstudy.info

Facebook.com/Newstudy.info

 

Stephens And Associates (Global Research and Product Testing)

3310 Keller Springs Rd # 130

Carrollton, TX 75006

 

 

 

 

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_____________________________________________________________________________________________________________________________________________________________________________________________________________________

 

 

5. D070- INFANT ECZEMA STUDY

 

SEEKING MALE & FEMALE INFANTS, AGES 2 MONTHS – 35 MONTHS, TO PARTICIPATE IN OUR UPCOMING CLINICAL RESEARCH STUDY

 

Study Objective:   This clinical trial is being conducted in order to evaluate the safety and efficacy of two creams in infants and toddlers with mild to moderate atopic dermatitis.

 

Eligibility:    Male & Female infants, ages 2 months to 35 months, with mild to moderate atopic dermatitis (eczema), and must have at least one active lesion to qualify.

 

Compensation:  Up to $230.00

Study Start Dates:  4/22

 

 

Visit: 1

Visit: 2

Visit: 3

Visit: 4

Visit: 5

Visit: 6

 

 

Group: 2

Last group!

22APR2014
Tuesday
5:00 PM - 6:30 PM

Anytime in between is ok

23APR2014
Wednesday
5:00 PM - 6:00 PM


24APR2014
Thursday
5:00 PM - 7:00 PM


25APR2014
Friday
5:00 PM - 7:00 PM


29APR2014
Tuesday
5:00 PM - 7:00 PM


06MAY2014
Tuesday
5:00 PM - 7:00 PM


 

 

 

All interested panelists must be screened and scheduled by Joanne Luu.

For consideration, please call: 

 

 

Joanne Luu

972-716-0630

Email: Joanne@newstudy.info

www.newstudy.info

Facebook.com/Newstudy.info

 

Stephens And Associates (Global Research and Product Testing)

3310 Keller Springs Rd # 130

Carrollton, TX 75006

 

 

cid:image002.jpg@01CF2BFA.EC86CF70

 

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6. D071- ACNE STUDY, OPEN FOR MALE AND FEMALE AGE 12-30 (Asian, Hispanic, Caucasian, African American).

MUST NOT BE IN ANY FACE STUDY PAST 4 WEEKS.

 

 

Acne Study

 

Thomas J. Stephens & Associates, Inc., a global research organization is seeking

 

MALES & FEMALES, AGES 12 - 30, WITH MILD TO MODERATE FACIAL ACNE

 

To participate in our upcoming research study.

 

Study Objective:   This clinical trial is being conducted in order to evaluate the efficacy and tolerance of the test product in subjects with mild to moderate acne vulgaris, through the assessment of its ability to quickly reduce the visible signs of existing pimples, reduce the numbers of acne lesions and improve the overall acne condition over time, as compared to the baseline appearance.

 

Eligibility:    Males & Females, ages 12 to 30, Fitzpatrick skin types 1 - 5, with mild to moderate facial acne. Prospective panelists must have between 10-50 inflammatory lesions AND 10-100 non-inflammatory lesions to qualify. 

 

Compensation:  Up to $350.00

Study Start Dates:  Saturday 4/26/14. (Everyone will be in the clinic all day, only Visit 1 will last up to 10 hours, the rest will be 1hr).

 

 

 

 

 

 

Visit: 1

Visit: 2

Visit: 3

Visit: 4

Visit: 5

Visit: 6

Visit: 7

Group: 2

26APR2014
Saturday
7:30 AM - 9am

 

Anytime between is ok.

Latest need to be at 9am.


27APR2014
Sunday
11:00 AM - 1:00 PM


28APR2014
Monday
4:30 PM - 6:30 PM


03MAY2014
Saturday
11:00 AM - 1:00 PM


10MAY2014
Saturday
12:00 PM - 2:00 PM


24MAY2014
Saturday
11:00 AM - 1:00 PM


21JUN2014
Saturday
11:00 AM - 1:00 PM


 

 

Number of Visit(s)

7

 

Length of Visits:

Visits 1: Up to 10 Hours

Visit 2 - 7:   1 Hour

 

Compensation

Up to $350.00

 

 

 

 

 

Notes

For Visit 1:

·        Subjects will NOT be allowed to leave the clinic

·        No smoke breaks will be allowed.

·        No small children are permitted.

·        Subjects are encouraged to bring something to read.

·        Personal music devices/DVD players are allowed (G – PG13 movies only) along with personal headset/earplugs.

·        Subjects are welcome to bring snacks and drinks if they wish.

·        Lunch will be provided.

 

 

All interested panelists must be screened and scheduled by Joanne Luu.

For consideration, please call: 

 

 

 

Joanne Luu

972-716-0630

Email: Joanne@newstudy.info

www.newstudy.info

Facebook.com/Newstudy.info

 

Stephens And Associates (Global Research and Product Testing)

3310 Keller Springs Rd # 130

Carrollton, TX 75006

 

 

 

 

 

 

 

 

 

 

NEW STUDY POSTED EVERY WEEK - PLEASE CHECK BACK SOON!

 

www.newstudy.info

 

cid:image002.jpg@01CF2BFA.EC86CF70

 

 

 

 

The following studies will be held only at ACRC.

 

Please contact ACRC directly to see if you qualify.

Tel:  (214) 379-2272 (ACRC)

 

Email: info@acrctrials.com

Website:  www.acrctrials.com or www.dfwstudy.com

Location:  Legacy Medical Village

 

5425 W. Spring Creek Parkway, Suite 130, Plano, TX 75024

 

 

ACRC is a network of award-winning physician practices and clinics located at Legacy Medical Village, a master planned facility that offers an opportunity for all patients and volunteers to safely participate in the evaluation of existing medications or new therapies which are not yet available for general use.  ACRC Trials has more investigators recognized by their peers as D Magazine “Best Doctors” then any other research facility in Texas.  Dallas Morning News also recently featured us in an article titled, “Plano Center May Be Model of the Future.”

 

Our mission is to provide exceptional services to our volunteers, and to set the standard of excellence in coordinating clinical trials to expedite the new drug development process so patients can enjoy the benefits of approved treatments as quickly as possible.

 

 

 

1. CONSTIPATION STUDY:

 

Are you experiencing CONSTIPATION due to your pain medication?

If you are 18-80 years of age and experiencing constipation caused by prescription pain medication, you may qualify to participate in a clinical research study.

All eligible study participants will receive:

 

ü    Comprehensive study related consultation with the study doctor

ü    Investigational drug or placebo (an inactive substance)

ü    Study-related visits, care, and monitoring.

 

 

Compensation up to $400 for travel may be provided

No cost to participate. No health insurance required.

Please contact us today to see if you qualify:

Tel: (214) 379-2272 (ACRC)

Email: info@acrctrials.com

Website: www.acrctrials.com / www.dfwstudy.com

Locations: Legacy Medical Village and Medical Center of Plano

Facebook: www.facebook.com/acrctrials

 

 

 

 

 

2. ASTHMA STUDY:

 

 

DO YOU or YOUR CHILD HAVE ASTHMA?

                         

      Are you at least 12 years of age?

 

Have you or your child:

                         

ü  Had asthma for at least 1 year? and

ü  Had an asthma attack requiring treatment in the past 12 months?

 

If so, you might qualify to participate in this 7 month research study evaluating two prescription asthma medications

                         

·         Participants will receive all study related medications, lung tests and office visit(s) at no charge.

·         Compensation for time and travel may be Provided

·         No Insurance is Necessary

 

 

For more information, contact:

(214) 379 – 2272 (ACRC)

 

www.DFWstudy.com

 

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The following studies will be held at Research Across America.

 

 

 

1. Hot Flashes Research Study - Suffering from hot flashes and sweating caused by menopause?  If you are a woman between the ages of 40 and 65 and are suffering from hot flashes and sweating due to menopause, you are invited to see if you may qualify for the REPLENISH Trial.  The purpose of this research study is to evaluate the safety and effectiveness of an investigational medication for menopause associated with hot flashes and sweating.

Each individual will be evaluated to determine her eligibility to participate in this study.  If you qualify, you will receive investigational study medication, study-related medical exams, and laboratory services at no charge.  You may also be reimbursed for time, travel, and other expenses.

In order to participate in the trial, women must be evaluated by a trial doctor and meet certain requirements including:

·         Being a female between the ages of 40 and 65

·         Being postmenopausal with an intact uterus

·         Be in generally good health

·         Be willing to participate in a clinical trial

If you would like to know more about setting up an appointment for pre-screening, please contact Research Across America at 972-4-DOCTOR (972-436-2867).  Or email us at study@raasites.com.

 

 

2. Plaque Psoriasis Research Study – If you have moderate symptoms of plaque psoriasis, including itchy, scaly, silvery-white and red patches on, you may qualify for a research study evaluating an investigational topical medication provided at no cost for up to 1 year (no placebo).  

·         Must be at least 18 years of age and have moderate plaque psoriasis

·         Have up to 20% body surface area affected with plaque psoriasis (excluding face and scalp)     

·         The study requires 15 visits over 1 year, with up to $900.00 compensation if you qualify.

 

This study is enrolling at our Plano location (Parker @ Tollway).  For information, call 972-4-DOCTOR972-4-DOCTOR.

 

 

 

 

 

 

 

 

 

 

Paid Study with RCTS- Irving, TX (Lot of openings for Male and Female, lot of great study going on now).

 

If you are a new panelist with RCTS, please email Joanne to request an application.

 

There must be a 4 pages application for NEW panelist to fill out first.

 

RCTS and Stephens and Associates are 2 different companies. (You can only do 1 study at a time).

 


3207 Esters Road
Irving, TX 75062

 

These are some of the studies going on at RCTS:

 

Panel 2812
250 MALE AND FEMALE SUBJECTS
NEEDED TO PARTICIPATE IN A CLINICAL RESEARCH PATCH STUDY INVOLVING
A CORTICOSTERIOD DRUG
*
Male and female subjects 18 to 65 years of age
*There will be up to 15 visits over approximately 8 weeks
*Payment for completing this study will be up to $175.00

 

 

Panel No. 3178
90 MALE & FEMALE SUBJECTS NEEDED
TO PARTICIPATE IN A CLINICAL RESEARCH STUDY INVOLVING
3 FACIAL CLEANSERS

*Male & Female subjects 18-35 years of age
*You must have at least 10 pimples on your face.
*There will be up to 4 visits over approximately 5 weeks
*Payment for completing this study will be up to $125

 

 

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If you are interested in any study listed ABOVE, Please call or reply to this email ONLYnewstudy@sbcglobal.net

 

Please put the study number on the SUBJECT LINE.


1. Name:

2. Home phone:

3. Work phone:

4. Cell phone:

5. Age & Race:

6. Name of study that you respond:

 

7. What other study are you participating at this time:

 

8. What date that you last finished a face usage study:

 

Please try to remember the study number and the date that you finish each study, it will make it easy when you sign up for the NEXT STUDY.

(The study number is listed on the pay check or the consent form).

 

 

Joanne Luu

972-716-0630

Email: newstudy@sbcglobal.net

 

Stephens and Associates (Clinical Study and Product Testing)

3310 Keller Springs Rd # 130

Carrollton, TX 75006

(near SW Intersection of Keller Springs and Midway)

 

 

 

 

 

 

Please pass these studies on to your friends or anyone who might be interested. We will have NEW studies listed every week!!

 

DISCLAIMER:

Please note that even though you may register for upcoming studies, you must still be screened and scheduled by your recruiter.

If you reply to a study, and do not hear back from us, that could mean the quota had been filled or you do not fit the requirement. Please be patient, and please keep trying for the next study. We will try our best to get you in a study that you best fit in.
 

 

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