Massage gun vs. hands: which eases Post-Hip-Surgery numbness?
NCT ID NCT07790705
First seen Aug 27, 2026 · Last updated Sep 09, 2026 · Updated 2 times
Summary
After hip replacement through a front incision, many people feel numbness, tingling, or burning in the thigh because a nearby nerve gets irritated. This trial tests whether a handheld massage gun, used at home twice a day for six weeks, can ease those symptoms faster than gentle hand massage. Adults scheduled for a first hip replacement will be randomly assigned to one of the two routines. Researchers will compare hip pain, function, numbness, and sleep quality at six weeks and three months after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A handheld percussive massage device (massage gun) self-applied to the thigh
- What this could lead to
- If it works, this could give hip replacement patients a simple, at-home way to recover faster and reduce lingering numbness and pain.
- What could go wrong
- This is a small, early-stage trial, and the massage gun may not outperform gentle hand massage. There is also a risk of discomfort or bruising from the device.
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
-
About 58 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Sep 2026
An estimate. Start dates often move.
- Expected to finish
-
Jan 2027
An estimate. End dates often move.
- Lead sponsor
-
A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Age 18 years or older at the time of surgery * Scheduled for primary unilateral elective anterior total hip arthroplasty for osteoarthritis, avascular necrosis, or inflammatory arthritis * Sufficient upper extremity strength and hand dexterity to perform either intervention independently, OR a reliable caregiver willing and able to assist with sessions throughout the 6-week period * Able to provide written informed consent * Willing and able to perform twice-daily sessions, maintain a daily log, and attend follow-up visits at Week 6 and Month 3 * Body mass index (BMI) less than 40 kg/m² Exclusion Criteria: * Revision arthroplasty or prior ipsilateral hip surgery * Pre-existing neurological condition affecting the ipsilateral anterior or lateral thigh, including peripheral neuropathy, lumbar L2-L4 radiculopathy, meralgia paresthetica, or diabetic amyotrophy * Confirmed or history of deep vein thrombosis or pulmonary embolism * Active wound infection, breakdown, dehiscence, or open incision at any treatment session timepoint * Coagulopathy, bleeding disorder, or supratherapeutic anticoagulation at time of enrollment * Active malignancy involving the hip or ipsilateral femur * Concurrent enrollment in another interventional trial * Significant cognitive impairment precluding safe self-administration or valid patient-reported outcome completion * Anticipated contralateral total hip arthroplasty within the 3-month follow-up window
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Avascular necrosis are added.
By submitting, you agree to our Terms of use
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Total Joint Specialists
Cumming, Georgia, 30041, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A prospective study using augmented reality versus conventional jig controls in total knee arthroplasty for osteoarthritis
- Can a purified form of ibuprofen better tame osteoarthritis pain?
- Could simple home exercises be the key to better knee health?
- Can a new plastic hip liner outlast the old ones?
- Which injection eases arm pain better: steroid or Anti-Inflammatory?
- A vast data bank could unlock secrets of bone and muscle diseases