A simple foot massage might ease pain and improve sleep after heart surgery
NCT ID NCT05567107
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This trial tests whether a 20-minute foot massage, given daily for three days after open heart surgery, can reduce pain, improve sleep quality, and boost mood. Adults undergoing coronary artery bypass grafting who report significant pain after surgery are randomly assigned to receive the massage or standard care. The study measures pain, anxiety, sleep, and mood using standard questionnaires to see if this gentle therapy aids recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Classical foot massage
- What this could lead to
- If effective, foot massage could become a simple, drug-free way to improve recovery after heart surgery, reducing pain and boosting sleep and mood.
- What could go wrong
- This is a small, early-stage trial, so results may not apply to everyone. Foot massage is generally safe but may not work for all patients or may have limited effect.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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84 people
The number who actually took part.
- Started
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Apr 2021
- Finished
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Sep 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Aged 18 years or older Scheduled to undergo elective coronary artery bypass grafting (CABG) surgery Voluntarily agreed to participate and provided informed consent Able to communicate verbally and understand the study procedures Hemodynamically stable following transfer from the intensive care unit to the cardiovascular surgery ward Reported a postoperative pain intensity of ≥4 on the Visual Analog Scale (VAS) Had no condition preventing the safe application of foot massage, including foot skin infection, local infection, open wound or lesion, significant edema or hematoma, thrombophlebitis, deep vein thrombosis, coagulation disorder, severe varicose veins, osteomyelitis, peripheral neuropathy, recent fracture, dislocation, or major musculoskeletal injury involving the lower extremities Exclusion Criteria: Development of a postoperative complication that prevented continuation of the intervention or study assessments Withdrawal of consent during the study Inability to complete the planned intervention or follow-up assessments
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Beyzanur Kızıloğlu
Erzurum, palandöken, 25000, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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