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Effect of a Village Doctor-delivered Exercise Therapy for Knee Osteoarthritis

4 czerwca 2026 zaktualizowane przez: Guanghua Lei, Xiangya Hospital of Central South University

Effect of a Village Doctor-delivered Exercise Therapy for Knee Osteoarthritis: a Pilot Feasibility Study

The goal of this clinical trial is to test the feasibility of village doctor-delivered exercise therapy for knee osteoarthritis in rural China, and to preliminarily explore its treatment effects. The main questions it aims to answer are:

  1. Is the exercise therapy delivered by village doctors feasible with satisfactory participant adherence?
  2. Can this intervention produce preliminary benefits in this small pilot sample? Researchers will compare village doctor-delivered exercise therapy to usual care to see if the intervention leads to greater pain relief and functional improvement in this pilot study.

Participants will complete village-delivered exercise therapy three times a week for 12 weeks, then maintain independent exercise for another 12 weeks or receive usual care for a total of 24 weeks.

Przegląd badań

Status

Zakończony

Warunki

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

16

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

  • Chiny
    • Hunan
      • Changsha, Hunan, Chiny, 410008
        • Xiangya Hospital, Central South University

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  1. aged 50-80 years;
  2. clinically diagnosed KOA according to the National Institute for Health and Care Excellence clinical criteria for OA (aged ≥45 years, activity-related knee pain, and either no morning joint-related stiffness or morning stiffness lasting no longer than 30 minutes);
  3. knee pain occurring on most days for over three months;
  4. the VAS pain score (range 0-10) ≥4;
  5. Kellgren-Lawrence (KL) grade of 2-3;
  6. residency in the designated village for the study duration.

Exclusion Criteria:

  1. have received intra-articular knee injections for pain within the past six months;
  2. have a history of knee surgery or have a planned knee replacement;
  3. have rheumatoid arthritis or other inflammatory joint diseases;
  4. possess physical or mental comorbidity that could interfere with the exercise regimen;
  5. have engaged in regular or organized exercise therapy within the past six months;
  6. are involved in an ongoing clinical trial

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Village doctor-delivered exercise
Participants allocated to the intervention group will receive village doctor-delivered exercise therapy.
Behawioralne: Exercise
The village doctor-delivered exercise program will be conducted over 12 weeks, with participants engaging in three sessions per week, each lasting approximately 50 minutes. To prevent excessive fatigue, each session will be scheduled with at least a one-day interval. Each session will consist of three phases: a warm-up phase, an exercise phase, and a cool-down phase. Following the 12-week exercise program supervised by village doctors, participants in the intervention group will be encouraged by researchers and village doctors to continue the exercise program without supervision until the 24-week follow-up.
Pozorny komparator: Usual care
Participants allocated to the control group will receive usual care, which means treat their knee condition as usual.
Behawioralne: Usual Care
Participants will seek medical attention and address their knee pain issues according to their past habits, but should not increase the use of previously unused treatment methods or adopt invasive treatment methods during the study period.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Visual Analogue Scale (VAS) of pain
Ramy czasowe: From baseline to 12-week follow-up
Changes in VAS pain score (range 0-10, with higher scores indicating greater pain) from baseline to 12-week follow-up
From baseline to 12-week follow-up
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) function score
Ramy czasowe: From baseline to 12-week follow-up
Changes in WOMAC function score (range 0-68, with higher score indicating more dysfunction) from baseline to 12-week follow-up
From baseline to 12-week follow-up

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Visual Analogue Scale (VAS) of pain
Ramy czasowe: From baseline to 6-week and 24-week follow-ups
Changes in VAS pain score (range 0-10, with higher scores indicating greater pain) from baseline to 6-week and 24-week follow-ups
From baseline to 6-week and 24-week follow-ups
WOMAC function score
Ramy czasowe: From baseline to 6-week and 24-week follow-ups
Changes in WOMAC function score (range 0-68, with higher score indicating more dysfunction) from baseline to 6-week and 24-week follow-ups
From baseline to 6-week and 24-week follow-ups
WOMAC pain score
Ramy czasowe: From baseline to 6-week, 12-week, and 24-week follow-ups
Changes in WOMAC pain score (ranges from 0 to 20, with higher scores indicating greater pain) from baseline to 6-week, 12-week, and 24-week follow-ups
From baseline to 6-week, 12-week, and 24-week follow-ups
WOMAC stiffness score
Ramy czasowe: From baseline to 6-week, 12-week, and 24-week follow-ups
Changes in WOMAC stiffness score (range 0-8, with higher score indicating more stiffness) from baseline to 6-week, 12-week, and 24-week follow-ups
From baseline to 6-week, 12-week, and 24-week follow-ups
WOMAC total score
Ramy czasowe: From baseline to 6-week, 12-week, and 24-week follow-ups
Changes in total WOMAC score (0-96, with higher score indicating worse symptoms and function) from baseline to 6-week, 12-week, and 24-week follow-ups
From baseline to 6-week, 12-week, and 24-week follow-ups
Patient global assessment (PGA)
Ramy czasowe: From baseline to 6-week, 12-week, and 24-week follow-ups
Changes in PGA score (range 0-10, with higher score indicating worse knee condition) from baseline to 6-week, 12-week, and 24-week follow-ups
From baseline to 6-week, 12-week, and 24-week follow-ups
12-Item Short Form Health Survey (SF-12)
Ramy czasowe: From baseline to 6-week, 12-week, and 24-week follow-ups
Changes in SF-12 score from baseline to 6-week, 12-week, and 24-week follow-ups. The SF-12 includes 12 items covering eight health domains and generates Physical Component Summary (PCS) and Mental Component Summary (MCS) scores on a 0-100 scale, with higher scores indicating better health-related quality of life
From baseline to 6-week, 12-week, and 24-week follow-ups
Knee synovitis
Ramy czasowe: From baseline to 12-week follow-up
Changes in knee synovitis (measured by ultrasound) from baseline to 12-week follow-up
From baseline to 12-week follow-up
Short Physical Performance Battery (SPPB)
Ramy czasowe: From baseline to 12-week follow-up.
Changes in SPPB score (range 0-12, with higher score indicating better physical performance) from baseline to 12-week follow-up
From baseline to 12-week follow-up.
Timed Up and Go (TUG) test
Ramy czasowe: From baseline to 12-week follow-up
Changes in TUG test from baseline to 12-week follow-up. The TUG test measures the time, in seconds, it takes for an individual to perform the following sequence of actions: stand up from a standard armchair (approximately 46 cm in seat height), walk a distance of 3 meters, turn, walk back to the chair, and sit down again. During the test, the participant wears their regular footwear and may use their customary walking aid, which can include none, a cane, or a walker. No physical assistance is provided. Fastest of two trials is recorded in seconds
From baseline to 12-week follow-up
30s chair stand test
Ramy czasowe: From baseline to 12-week follow-up
Changes in 30s chair stand test from baseline to 12-week follow-up. For the 30s chair stand test, participants are asked to fold their arms across their chest and to stand up from the chair one time. If successful, participants will be asked to stand up and sit down within 30 seconds as quickly as possible. The total number of stands executed correctly within 30s is recorded.
From baseline to 12-week follow-up
6-meter walking test
Ramy czasowe: From baseline to 12-week follow-up
Changes in 6-meter walking test from baseline to 12-week follow-up. In the 6-meter walking test, we measure the time it took to walk 6 meters at a regular pace, starting from a moving position, without slowing down, and then calculate the average of 2 tests.
From baseline to 12-week follow-up
Muscle thickness of quadriceps muscle
Ramy czasowe: From baseline to 12-week follow-up
Changes in muscle thickness of quadriceps muscle (measured by ultrasound) from baseline to 12-week follow-up
From baseline to 12-week follow-up
Muscle quality of quadriceps muscle
Ramy czasowe: From baseline to 12-week follow-up
Changes in muscle quality of quadriceps muscle (measured by ultrasound) from baseline to 12-week follow-up
From baseline to 12-week follow-up
Grip strength
Ramy czasowe: From baseline to 12-week follow-up
Changes in grip strength from baseline to 12-week follow-up. Grip strength is measured using a calibrated JAMAR hydraulic hand dynamometer (Lafayette Instruments). Participants are positioned sitting upright in a stable four-legged chair (no armrests) with thighs horizontal and at 90°. The assessed arm is bent with the upper arm vertical, lower arm horizontal, elbow tight into the waist and the non-assessed arm placed relaxed in their lap. Three measurements are taken at 10-second intervals for each hand and the averaged value of the three measurements is used as the final grip strength for each hand
From baseline to 12-week follow-up
Quadriceps muscle strength
Ramy czasowe: From baseline to 12-week follow-up
Changes in quadriceps muscle strength from baseline to 12-week follow-up. The maximum voluntary quadriceps contraction is assessed for each participant in a standard fashion using the 'Nicholas Manual Muscle Tester' (Lafayette Instruments). The participant is positioned sitting upright on a stable flat surface (no arm rests) with thighs horizontal and knees at 90° flexion. The instrument is then positioned at the bottom of the participant's tibia just above the ankle and they are asked to push against it as hard as possible in an attempt to raise their lower leg forwards, with resistance provided by the research metrologist. This is carried out three times on each leg and the mean value for each side is recorded
From baseline to 12-week follow-up
Hamstring muscle strength
Ramy czasowe: From baseline to 12-week follow-up
Changes in hamstring muscle strength from baseline to 12-week follow-up. The maximum voluntary hamstrings muscle strength is assessed for each participant in a standard fashion using the 'Nicholas Manual Muscle Tester' (Lafayette Instruments). Participants are tested in prone for three repetitions with the test knee at 90° flexion and with the dynamometer placed immediately proximal to the level of the prominence of the lateral malleolus. Tests are performed alternating between the dominant and non-dominant limb. The mean value of three testing for each side is recorded
From baseline to 12-week follow-up
Quantitative sensory testing (QST)
Ramy czasowe: From baseline to 12-week follow-up
Changes in QST from baseline to 12-week follow-up. Pressure pain threshold (PPT) is assessed to represent quantitative sensory. An algometer (1 cm2 rubber tip; Wagner, FDIX25) is applied at a rate of 0.5 kg/second on each anatomical site and determining the point at which participants verbally indicated the pressure first changed to slight pain. Participants are familiarised before testing by twice PPT testing on sternal notch. The PPT testing is conducted at 9 sites: sternum (3-cm caudal to the sternal notch), the medial and lateral tibiofemoral joint lines adjacent to the patellar ligament of each knee, the proximal tibia (5-cm distal to the tibial tuberosity of each leg), and the centre of the patella
From baseline to 12-week follow-up
Hip abductor muscle strength
Ramy czasowe: From baseline to 12-week follow-up
Changes in hip abductor muscle strength from baseline to 12-week follow-up. The maximum voluntary hip abductor muscle contraction is assessed for each participant in a standard fashion using the 'Nicholas Manual Muscle Tester' (Lafayette Instruments). The participant is positioned on a clinic couch lying on their side with the lower leg bent for stability and the upper leg out straight. The instrument is then positioned above the lateral condyle of femur and the participant are asked to push against it as hard as possible in an attempt to raise their leg up towards the ceiling with resistance provided by the researcher. This is carried out three times on each leg and the mean value for each side is recorded
From baseline to 12-week follow-up
Appendicular skeletal muscle mass
Ramy czasowe: From baseline to 12-week follow-up
Changes in appendicular skeletal muscle mass from baseline to 12-week follow-up. The participant had their appendicular skeletal muscle mass measured using bioimpedance analyses (InBody 770 analyser, InBody Japan, Tokyo, Japan). With bare feet, the participants are instructed to stand with heel and forefoot placed on the metal plates of the instrument and grab the handle. A sub-threshold electrical current is then transmitted through the body from foot to foot. The impedance-based appendicular skeletal muscle mass is determined as per the manufacturer's imbedded equations
From baseline to 12-week follow-up
Body fat percentage
Ramy czasowe: From baseline to 12-week follow-up
Changes in body fat percentage from baseline to 12-week follow-up. The participant had their body fat percentage measured using bioimpedance analyses (InBody 770 analyser, InBody Japan, Tokyo, Japan). With bare feet, the participants are instructed to stand with heel and forefoot placed on the metal plates of the instrument and grab the handle. A sub-threshold electrical current is then transmitted through the body from foot to foot. The impedance-based body fat percentage is determined as per the manufacturer's imbedded equations
From baseline to 12-week follow-up

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Xiangya Hospital of Central South University

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

3 lipca 2025

Zakończenie podstawowe (Rzeczywisty)

28 września 2025

Ukończenie studiów (Rzeczywisty)

20 grudnia 2025

Daty rejestracji na studia

Pierwszy przesłany

26 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

4 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

10 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

10 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • 202505062

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Opis planu IPD

This is a small-sample pilot feasibility study. We have no plan to share individual participant data (IPD) externally. Considering the limited sample size, participant privacy protection and institutional ethical requirements, the raw individual data will not be released to external researchers.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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