A Study to Analyse the Immediate Effect of Dry Needling and Extra Corporeal Shock Wave Therapy on Hand Grip Strength
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| ClinicalTrials.gov Identifier: NCT04645758 |
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Recruitment Status :
Recruiting
First Posted : November 27, 2020
Last Update Posted : December 1, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Muscle Weakness Condition | Combination Product: Dry needling and Extra corporeal Shock wave therapy | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 27 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | Participants will be assigned to two groups in parallel for the duration of the study. |
| Masking: | Single (Outcomes Assessor) |
| Masking Description: | M.M.K outcome blind assessor |
| Primary Purpose: | Health Services Research |
| Official Title: | The Immediate Effects of Dry Needling and Extra Corporeal Shockwave Therapy on Hand Grip Strength.A Randomised Controlled Trail. |
| Actual Study Start Date : | November 29, 2020 |
| Actual Primary Completion Date : | November 29, 2020 |
| Estimated Study Completion Date : | November 29, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: Dry Needling Group or (DN)
Dry needling for 5 mins on the flexor group of muscles of dominant forearm.
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Combination Product: Dry needling and Extra corporeal Shock wave therapy
5 mins of dry needling and 1250 pulses of shockwave therapy on dominant forearm muscles
Other Name: Dry needle/Acupuncture needle.Shock wave therapy |
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Active Comparator: Extra corporeal Shockwave therapy Group or (ESWT)
Delivering of Shock wave pulses of 1250 at the energy intensity of 0.58 mj/mm2 on the flexor group of muscles of dominant forearm
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Combination Product: Dry needling and Extra corporeal Shock wave therapy
5 mins of dry needling and 1250 pulses of shockwave therapy on dominant forearm muscles
Other Name: Dry needle/Acupuncture needle.Shock wave therapy |
- Hand Grip Strength [ Time Frame: Post 1 hours of Intervention in both groups ]Measurement of Hand Grip Strength with Jamar Dynamometer
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| Ages Eligible for Study: | 21 Years to 46 Years (Adult) |
| Sexes Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- No pain on the visual analog scoring scale of 100 mm scale,
- Muscle power of 4+ on oxford manual muscle testing of forearm and wrist extrinsic and intrinsic muscles
- Full range of motion in all dominant upper extremity joints.
Exclusion Criteria:
- History of previous fractures of the dominant upper extremity,
- Teno-synovitis of flexor tendons ,
- Dequervains synovitis,
- Left hand dominance.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04645758
| Contact: Mohammed A Khan, BPT | 00966508921749 | amjadkhan.mmkk@gmail.com | |
| Contact: Rayan M Fadani, BPT | 00966500600065 | dr.rayanalfadani@gmail.com |
| Saudi Arabia | |
| Comprehensive Rehabilitation Centre | Recruiting |
| Medina, Saudi Arabia, 42381 | |
| Contact: Mohammed A Khan 0508921749 amjadkhan.mmkk@gmail.com | |
| Principal Investigator: Rayan M Al-Fadani, BPT | |
| Sub-Investigator: Ibrahim H Al-Tobaigy, BPT | |
| Sub-Investigator: Mujahid M Khoja, MBBS | |
| Sub-Investigator: Mohammed A Khan, BPT | |
| Sub-Investigator: Abdullah M Al-Shenqiti, PhD | |
| Sub-Investigator: Tarek M El-Gohary, PhD | |
| Principal Investigator: | Rayan M Al-Fadani, BPT | Comprehensive rehabilitation centre, Medina Al Munawwarah, Saudi Arabia. | |
| Study Director: | Abdullah M Al-Shenqiti, PhD,PT | Taibah University of Medical Rehabilitation Sciences | |
| Study Chair: | Tarek M El-Gohary, PhD,PT | Taibah University of Medical Rehabilitation Sciences |
| Responsible Party: | Rayan Mohammed Al Fadani, Head of the Department of Physical therapy and Rehabilitation., Comprehensive Rehabilitation Centre, Medina, Saudi Arabia |
| ClinicalTrials.gov Identifier: | NCT04645758 |
| Other Study ID Numbers: |
Rct001 |
| First Posted: | November 27, 2020 Key Record Dates |
| Last Update Posted: | December 1, 2020 |
| Last Verified: | November 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Plan Description: | Results of Hand grip strength pre and post intervention. |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Dry needling Extra corporeal Shockwave therapy Hand Grip Strength Post 1 hour |
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Muscle Weakness Muscular Diseases Musculoskeletal Diseases Neuromuscular Manifestations |
Neurologic Manifestations Nervous System Diseases Pathologic Processes |

