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Trial · NCT07883863

Impact of Range of Motion Exercises on Pain and Functional Ability

NCT07883863, Not applicable, Not yet recruiting, Al-Azhar University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Impact of Range of Motion Exercises on Pain and Functional Ability. Trials, record NCT07883863. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07883863

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Impact of Range of Motion Exercises on Pain and Functional Ability
NCT number
NCT07883863
Status
Not yet recruiting
Phases
Not applicable
Enrollment
80 participants, estimated
Lead sponsor
Al-Azhar University
Conditions
Impact of ROM Exercises on Pain and Functional Ability in Patients With Second -Degree Burns
Interventions
Range of Motion exercises
First posted
2026-10-20
Last updated
2026-10-20

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPatient's Structured Interview QuestionnaireBaseline assessment before the intervention
It will be divided into two parts and written in the Arabic language. Part 1: Patient's demographic characteristics It aims to assess patient' age, gender, marital status, degree of education …. etc. Part 2: Medical health profile It aims to assess information on the patient's present history, past history. It will include cause of burn, degree of burn, percent of burn, first aid, skin graft, limb affected, date of admission and date of discharge.
PrimaryChange in Pain IntensityBaseline assessment before the intervention and follow-up assessment at the end of 3 weeks.
Pain Numeric Rating Scale It will be used to assess the patient's level of pain through asked the patient to make four pain ratings from 0 to 10 score, corresponding to current, no pain, mild, moderate and severe pain experienced. Scoring system * 0 (no pain) * 3 (mild pain) * 4 - 6 (moderate pain) * 7- 10 (severe pain)
PrimaryChange in Functional Ability of the Affected upper ExtremitiesBaseline and 3 weeks after the intervention
Upper Extremity Functional Index (UEFI) It will be used to assess upper extremities functional abilities of patients with burn injury in performing activities of daily living. The scale lists 20 activities, and the patient gives a score to each based on the difficulty they have completing that activity. The maximum possible score is 80 points, indicating very high function. The minimum possible score is 0 points, indicating very low function. This scale has 5-point rating scale, ranging from 0 to 4. 0 indicates extreme difficulty or unable to perform activity while 4 indicates no difficulty. A lower score indicates that the person is reporting increased difficulty with the daily activities as a result of their limb condition. * (0 - 9) extreme extremity functional limitation. * (10 - 31) severe extremity functional limitation. * (32 - 52) moderate extremity functional limitation. * (53 - 79) mild extremity functional limitation. * (80) no extremity functional limitation.
PrimaryChange in Functional Ability of the Affected lower ExtremitiesBaseline and 3 weeks after the intervention
Lower Extremity Functional Scale (LEFS) It will used to assess the functional limitation of a patient with lower extremities burn injury. The scale lists 20 activities, and the patient gives a score to each based on the difficulty they have completing that activity. This scale has 5-point rating scale, ranging from 0 to 4. 0 indicates extreme difficulty or unable to perform activity while 4 indicates no difficulty. A lower score indicates that the person is reporting increased difficulty with the daily activities as a result of their limb condition. * (0 - 9) extreme extremity functional limitation. * (10 - 31) severe extremity functional limitation. * (32 - 52) moderate extremity functional limitation. * (53 - 79) mild extremity functional limitation. * (80) no extremity functional limitation.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07883863

GET https://conductscience.org/api/trials/v1/NCT07883863/registered