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NCT Number: NCT06786884

Paraffin Wax and Exercise Prospective

This study is being done to test if paraffin wax can be used to improve the range of motion and function for scars across joints when used in combination with scar rehabilitation therapy sessions. For those randomized to receive it, the paraffin wax will be used alongside the participants' exercise therapy treatments. Currently, treatments that are used in addition to rehabilitation therapy for increasing range of motion across joints in the burn population are limited. By getting more information about how paraffin wax may or may not work, patients in the future that have scars may be able to be helped.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

MedStar Washington Hosptial Center

Washington D.C., District of Columbia, 20010, United States

Location status: Recruiting

Location contact

Bonnie C Carney, PhD

PRINCIPAL_INVESTIGATOR

Clinical Research Coordinator

CONTACT

[email protected]

202-877-5170

About this study

If the participants agree to take part in this study, the participants scars will be looked at and the investigators will select one site that will be involved in the research. The scar will be "randomized" to the paraffin wax or no paraffin wax groups. The treatment the participants get will be chosen by chance, like flipping a coin. Neither the participants nor the study doctor will choose what treatment you get. The participants will have a 50% chance of being given either paraffin wax or not.

The study will take place in an outpatient setting. The participants will not be admitted to the hospital overnight. All patients who enter the study will be required to follow-up for regular appointments with their burn department.

Before the participants begin treatment, the participants will come in for a pre-treatment visit where the investigators will collection information about the participants scars such as pictures, range of motion measurements, non-invasive probes, non-invasive imaging (Laser doppler imaging) and questionnaires. These questionnaires will be related to the symptoms, range of motion, function, and appearance of the participants' burn scars. At the pre-treatment visit, there is an also an optional blood draw where less than 2 tablespoons of blood are collected. It is estimated this visit will take less than 1 hour. The investigators will also collect information from the medical record about prior surgical and medical history.

Exercise treatments (which the participants have previously chosen to undergo in talking with the participants doctor) will occur approximately in 1-2-week intervals depending on what the Burn Center scheduling department allows. For completion of this study, the participants will undergo 4 exercise therapy sessions which may take about 8 weeks.

At each visit, the following measurements will be captured before and after each exercise session. Those assigned to the paraffin wax group will have an additional assessment collected before their exercise therapy session and after the paraffin wax has been removed. Measurements at each visit include active and passive range of motion measurements of the affected joint, non-invasive probe measurements to measure water loss and hardness of your scar and the adjacent area of normal skin, digital photography, non-invasive laser doppler imaging (LDI), surface-level skin temperature measurements using either an infrared thermometer or skin temperature strip as well as pain and itch rating scales.

When applicable, the paraffin wax will be applied to the top of the scar for 15 minutes and repeat measurements previously listed above will be collected before your standard of care rehabilitation session. These sessions conducted by the burn rehab therapist may include scar massage, exercises, and functional activity. Specific treatments will be documented.

At each study visit, photographs will be taken of the study designated scar. All photographs taken for the purpose of this study will be taken by a high-resolution study camera. Photographs will be labeled with your study ID number. All efforts will be made to minimize the amount of identifiable information such as the participants' face or tattoos in these photos.

The procedures/treatments in this study that are considered experimental/investigation are: the use of the study product (paraffin wax) to assess the effect on burn scar that crosses an extremity joint during rehabilitation exercises.

The following procedures are part of the research study and would not normally be done as part of routine care: study provided paraffin wax and control application to the scar, scar assessments, digital photography, LDI, non-invasive imaging and measurements. These procedures are part of the study and will not be charged to insurance.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Patients with burn scar that crosses an upper or lower extremity joint (shoulder, elbow, wrist, hand, hip, knee, ankle)
  • Patients that have been prescribed a rehabilitation program where paraffin wax could be used as an adjunct to rehab exercise therapy

Exclusion criteria

  • Adults unable to provide informed consent
  • Injury etiology other than burn (ex: cutaneous trauma, cold injury, etc.)
  • Pregnant women
  • Prisoners

Treatment and study plan

paraffin wax

Device

This is the treatment group that will receive exercise and paraffin wax

standard of care exercise therapy

Device

This is the group that will only receive exercise therapy and no paraffin wax.

Primary outcomes

  1. Range of motion

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Range of motion (degrees) of the affected joint before and after paraffin wax between the paraffin and no paraffin groups

Secondary outcomes

  1. Trans-epidermal water loss

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Trans-epidermal water loss (TEWL)(kg/m2h) of the HTS before and after paraffin wax between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 100 Higher score is a worse outcome.

  2. Stiffness

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Scar elasticity/hardness/stiffness by durometry (N/m) of the HTS before and after paraffin wax between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 300 Higher score is a worse outcome.

  3. Pain visual analog scale

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Pain visual analog scales (score) before and after paraffin wax between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 100 Higher score is a worse outcome.

  4. Itch visual analog scale

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Itch visual analog scales (score) before and after paraffin wax between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 100 Higher score is a worse outcome.

  5. Scar surface temperature

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Scar surface temperature (degrees celsius) before and after paraffin wax by scanner between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 100 Higher score is a worse outcome.

  6. Patient and observer scar assessment scale

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    Pre and Post Study Patient and observer scar assessment scale (POSAS) version 3.0 pre and post paraffin at the first session and session four between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 10 Higher score is a worse outcome.

  7. Perfusion

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    •Laser doppler imaging of perfusion (perfusion units) before and after paraffin wax first session only between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 500 Higher score is a worse outcome.

  8. Lower extremities functional scale

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    • Pre (session 1) and Post (final session) study Lower extremity functional scale (LEFS) (score) between the paraffin and no paraffin groups.

    Minimum: 0 Maximum: 80 Lower score is a worse outcome.

  9. Disabilities of the shoulder and hand

    Time frame: 4th exercise session, an average of 4 weeks post enrollment

    • Pre (session 1) and Post (final session) study disabilities of the arm, shoulder, and hand (DASH) (score) between the paraffin and no paraffin groups.

    Minimum: 30 Maximum: 150 Higher score is a worse outcome.

Sponsors and collaborators

Lead sponsor

Medstar Health Research Institute

Other

Registry information

Official study title

A Pilot, Randomized Controlled Trial Evaluating the Effectiveness of Paraffin Wax On Burn Patient Function, Range of Motion and Scar

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jan 22, 2025
Registry last updated
Jun 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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