Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D029424', 'term': 'Pulmonary Disease, Chronic Obstructive'}], 'ancestors': [{'id': 'D008173', 'term': 'Lung Diseases, Obstructive'}, {'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D002908', 'term': 'Chronic Disease'}, {'id': 'D020969', 'term': 'Disease Attributes'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D026201', 'term': 'Musculoskeletal Manipulations'}], 'ancestors': [{'id': 'D000529', 'term': 'Complementary Therapies'}, {'id': 'D013812', 'term': 'Therapeutics'}, {'id': 'D026741', 'term': 'Physical Therapy Modalities'}, {'id': 'D012046', 'term': 'Rehabilitation'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 52}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2023-03-20', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2024-04', 'completionDateStruct': {'date': '2024-03-01', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2024-04-07', 'studyFirstSubmitDate': '2023-01-21', 'studyFirstSubmitQcDate': '2023-03-22', 'lastUpdatePostDateStruct': {'date': '2024-04-09', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2023-03-23', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2024-01-01', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'chest expansion', 'timeFrame': 'pre-intervention and after 8 weeks of intervention', 'description': 'caliper will be used to assess chest expansion into centimeter'}, {'measure': '(the forced vital capacity (FVC), forced expiratory volume at first second (FEV1) and FEV1/FVC will be recorded. )', 'timeFrame': 'pre-intervention', 'description': 'spirometry used to measure'}, {'measure': 'cranio-vertebral angle and kyphotic angle in degrees', 'timeFrame': 'pre-intervention', 'description': 'kinovea software will be used to assess in degrees'}, {'measure': 'functional capacity.', 'timeFrame': 'pre-intervention', 'description': 'Six minute walk test will be used to assess functional capacity(meter/minutes)'}, {'measure': 'dyspnea score', 'timeFrame': 'pre-intervention', 'description': 'Modified Medical Research Council dyspnea scale (mMRC dyspnea scale) will be used to assess dyspnea'}]}, 'oversightModule': {'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Chronic Obstructive Pulmonary Disease']}, 'descriptionModule': {'briefSummary': 'Our study aiming for determining the combined effect of selective manual therapy techniques in chronic obstructive pulmonary disease patients', 'detailedDescription': 'I will apply selective manual therapy techniques in form of mobilization techniques ,myofascial release techniques combined with traditional treatment to determine thier effect in chronic obstructive pulmonary disease patients'}, 'eligibilityModule': {'sex': 'MALE', 'stdAges': ['ADULT'], 'maximumAge': '60 Years', 'minimumAge': '50 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* All patients must diagnosed mild to moderate chronic obstructive pulmonary disease\n* All patients should have foreward head and kyphosis\n\nExclusion Criteria:\n\n* History of osteoporosis.\n* Acute exacerbation.\n* Presence of active hemoptysis\n* Presence of malignant disease'}, 'identificationModule': {'nctId': 'NCT05781867', 'briefTitle': 'Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease', 'organization': {'class': 'OTHER', 'fullName': 'Cairo University'}, 'officialTitle': 'Effect of Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease', 'orgStudyIdInfo': {'id': 'manual therapy in COPD'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'PLACEBO_COMPARATOR', 'label': 'control', 'description': '26patients will be included in this group and will receive conventional physiotherapy in form of pursed lip breathing, diaphragmatic breathing exercise and Active Range of Motion of both upper extremities', 'interventionNames': ['Other: Manual therapy and conventional physical therapy treatment']}, {'type': 'EXPERIMENTAL', 'label': 'manual therapy', 'description': '26patients will be included in this group and will receive manual therapy (chest mobilization, diaphragmatic myofascial release, myofascial release for pectoralis minor and major, scaleni ) and conventional physiotherapy', 'interventionNames': ['Other: Manual therapy and conventional physical therapy treatment']}], 'interventions': [{'name': 'Manual therapy and conventional physical therapy treatment', 'type': 'OTHER', 'description': 'manual therapy (chest mobilization, diaphragmatic myofascial release, myofascial release for pectoralis minor, pectoralis major, scaleni ),pursed lip breathing, diaphragmatic breathing and active range of motion exercises of upper limbs', 'armGroupLabels': ['control', 'manual therapy']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Giza', 'country': 'Egypt', 'facility': 'Cairo University', 'geoPoint': {'lat': 30.00944, 'lon': 31.20861}}]}, 'ipdSharingStatementModule': {'ipdSharing': 'UNDECIDED', 'description': 'waiting to know the results of the intervention'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Cairo University', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'M.SC physical theray', 'investigatorFullName': 'Amira saad mohamed', 'investigatorAffiliation': 'Cairo University'}}}}