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At a Glance
Age
18 – 85
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
24 (estimated)
Sponsor
Jill Cole · Other
Who this trial is looking for
This trial is looking for patients with gynecologic cancer who are receiving infusion treatments. Participants will either receive massage therapy or an attention control during their treatment sessions.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with gynecologic cancer.
I am receiving active treatment involving infusion.
This is my first time undergoing infusion therapy.
You may not be able to join if
I have received infusion therapy within the past 2 years.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this clinical trial is to determine the feasibility of studying massage therapy in patients with gynecologic cancers while receiving infusion treatments. The central hypothesis is that it is feasible to implement a massage intervention study in an infusion center at an academic hospital, and measure pain and anxiety in patients with gynecological cancer. The main questions it aims to a…
The goal of this clinical trial is to determine the feasibility of studying massage therapy in patients with gynecologic cancers while receiving infusion treatments. The central hypothesis is that it is feasible to implement a massage intervention study in an infusion center at an academic hospital, and measure pain and anxiety in patients with gynecological cancer. The main questions it aims to answer are:
Can investigators evaluate feasibility to conduct a study from a design standpoint? Can investigators assess the use of randomization, blinding of assessors, potential to control the study with an attention group, and recruitment/retention processes? Can investigators successfully collect outcome measures of pain and anxiety, pre/post intervention? Researchers will investigate degree of resources needed, such as massage therapists, assessors, and timing of delivery intervention. Assess positive/negative effects on target population determining massage modality and anatomical location. Researchers will compare massage therapy to an attention control group, to see if massage therapy works to treat pain and anxiety in patients with cancer.
Establish variability in outcome measures.
Participants will:
Be randomized and receive either massage therapy or attention control over the course of three consecutive infusion therapy treatments. Each infusion therapy treatment occurs every 2-4 weeks.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with gynecologic cancer receiving active treatment of infusion, including but not limited to chemotherapy, immunotherapy, antibiotics, and blood.
* Patients with gynecological cancer undergoing an infusion for the first time.
Exclusion Criteria:
* Patient with gynec…
Inclusion Criteria:
* Patients with gynecologic cancer receiving active treatment of infusion, including but not limited to chemotherapy, immunotherapy, antibiotics, and blood.
* Patients with gynecological cancer undergoing an infusion for the first time.
Exclusion Criteria:
* Patient with gynecologic cancer that has received infusion therapy anytime within the past 2 years.
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