Case Study

Menopause Case Study

A global consumer packaged goods company wanted to understand the effectiveness of an herbal blend on menopause symptoms and quality of life (QoL).

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

A global consumer packaged goods company wanted to understand the effectiveness of an herbal blend on menopause symptoms and quality of life (QoL).

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

Men's/Women's Health
Assessing the impact of a new treatment for menopausal symptoms.

87%

Retention Rate

86%

Study Product Adherence

130

Women Enrolled

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

A global consumer packaged goods company wanted to understand the effectiveness of an herbal blend on menopause symptoms and quality of life (QoL).

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

A global consumer packaged goods company wanted to understand the effectiveness of an herbal blend on menopause symptoms and quality of life (QoL).

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate

Case Study

Menopause Case Study

A global consumer packaged goods company wanted to understand the effectiveness of an herbal blend on menopause symptoms and quality of life (QoL).

Men's/Women's Health

Challenge

A global consumer packaged goods company needed clinical evidence on the effectiveness of an herbal blend for relieving menopause symptoms and improving quality of life (QoL), including hard-to-quantify symptoms like hot flashes.

‍

Solution

The randomized, double-blind, placebo-controlled study was conducted fully remotely with no physical research site. Apart from two local lab blood draws, participants completed all study procedures in-app. 130 women consumed the study product daily, updated e-diaries, and completed digital questionnaires at weekly intervals. One-touch, real-time ePRO reporting reduced recall bias, and a dedicated "hot flash indicator" button let participants log each episode as it happened, giving the sponsor rich data on hot flash frequency and severity. Changes from baseline were assessed over 12 weeks.

‍

Results

• The study delivered complete, analyzable efficacy and safety data over 12 weeks, with significant improvement from baseline in hot flash frequency and severity
• Regular notifications and study-team follow-up kept participants engaged
• Ease of in-app reporting contributed to an 87% retention rate