UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057282
Receipt number R000065480
Scientific Title Effects of exercise therapy on postherpetic neuralgia: a single-arm trial
Date of disclosure of the study information 2025/04/01
Last modified on 2025/03/13 22:38:14

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Basic information

Public title

Effects of exercise therapy on postherpetic neuralgia

Acronym

Effects of exercise therapy on postherpetic neuralgia

Scientific Title

Effects of exercise therapy on postherpetic neuralgia: a single-arm trial

Scientific Title:Acronym

Effects of exercise therapy on postherpetic neuralgia: a single-arm trial

Region

Japan


Condition

Condition

Postherpetic neuralgia

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to evaluate the effects of exercise therapy on postherpetic neuralgia.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Brief pain inventory, douleur neuropathique 4 questions, neuropathic pain symptom inventory

Key secondary outcomes

Mechanical detection threshold, mechanical pain threshold, mechanical pain sensitivity, temporal summation of pain, conditioned pain modulation, pain catastrophizing scale, hospital anxiety and depression scale, EuroQOL 5 dimentions 5-level


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Supervised exercise therapy

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

50 years-old <=

Age-upper limit

90 years-old >

Gender

Male and Female

Key inclusion criteria

At least 90 days post-onset of herpes zoster.
Undergoing pharmacological therapy and nerve block.
The average pain score in the BPI remains at or above 4.

Key exclusion criteria

Patients with postherpetic neuralgia of the lower extremities, cognitive dysfunction that would affect the examination, and severe cardiac, respiratory, or metabolic diseases.
Pregnant women.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Takako
Middle name
Last name Matsubara

Organization

Kobe Gakuin University

Division name

Department of Rehabilitation

Zip code

651-2180

Address

Arise 518, Ikawadani-cho, Nishi-ku, Kobe

TEL

(078)974-1551

Email

matsubar@reha.kobegakuin.ac.jp


Public contact

Name of contact person

1st name Takako
Middle name
Last name Matsubara

Organization

Kobe Gakuin University

Division name

Department of Rehabilitation

Zip code

651-2180

Address

Arise 518, Ikawadani-cho, Nishi-ku, Kobe

TEL

(078)974-1551

Homepage URL


Email

matsubar@reha.kobegakuin.ac.jp


Sponsor or person

Institute

Kobe Gakuin University

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor

None

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kobe Gakuin University

Address

Ikawadani-cho, Nishi-ku, Kobe

Tel

(078)974-1551

Email

ethic@reha.kobegakuin.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

牧港クリニック(沖縄県)


Other administrative information

Date of disclosure of the study information

2025 Year 04 Month 01 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Preinitiation

Date of protocol fixation

2024 Year 11 Month 19 Day

Date of IRB


Anticipated trial start date

2025 Year 04 Month 01 Day

Last follow-up date

2028 Year 03 Month 31 Day

Date of closure to data entry

2028 Year 03 Month 31 Day

Date trial data considered complete

2028 Year 04 Month 01 Day

Date analysis concluded

2028 Year 06 Month 30 Day


Other

Other related information



Management information

Registered date

2025 Year 03 Month 13 Day

Last modified on

2025 Year 03 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065480