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Clinical Trials/CTRI/2025/07/091239
CTRI/2025/07/091239Not yet recruitingPhase 2

Effects of Proprioceptive Neuromuscular Facilitation on Pain, Neck Proprioception, and Sleep Quality in Individuals with Cervicogenic Headache.

Prashant Kumar1 site in 1 country36 target enrollmentStarted: July 31, 2025Last updated:

Trial Snapshot

Phase
Phase 2
Status
Not yet recruiting
Sponsor
Enrollment
36
Locations
1
Primary Endpoint
Headache Impact Test-6 (HIT-6)

Study Overview

Brief Summary

Cervicogenic headache, originating from cervical spine dysfunction, significantly impact individuals’ quality of life. Proprioceptive Neuromuscular Facilitation (PNF) is a therapeutic technique that may enhance proprioception, balance, and overall well-being. This study investigates the effects of PNF on pain, neck proprioception, and sleep quality in individuals with cervicogenic headache. To investigate the effects of Proprioceptive Neuromuscular Facilitation (PNF) on Pain, Neck proprioception and sleep quality in individuals suffering from cervicogenic headache.  Total 36 patients will be recruited on the basis of inclusion and exclusion criteria. Subjects will be allocated in Experimental group (a single group pre – post design) with purposive sampling technique. Outcome measure will be assessed at two time points: Baseline and Post- Intervention (Immediately after the completion of Six-week PNF treatment). The PNF techniques will include PNF patterns of neck and techniques including rhythmic stabilization, contract-relax and hold-relax, targeting the cervical region and associated musculature. Pain will be assessed by Headache Impact Test-6 (HIT-6), Neck proprioception will be evaluated using a repositioning error test, and sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI). Participants will undergo PNF treatment for 30 minutes, three times a week for six weeks.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 35.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Age 18-35 years Both males and females Patient having cervicogenic headache as diagnosed by International Study Group Criteria (CHISG).

Exclusion Criteria

  • Subjects with recent history of surgery of Brain Traumatic Neck Injury Patient who has undergone physiotherapy intervention within last 3 months Individuals having headache due to migraine.
  • Individuals having any fracture of cervical spine, osteoporosis, cervical stenosis, tumor, uncontrolled hypertension, prolonged use of steroid.

Outcomes

Primary Outcomes

Headache Impact Test-6 (HIT-6)

Time Frame: Baseline, Post-intervention (6 weeks)

Cervical Joint Position error test (JPET)

Time Frame: Baseline, Post-intervention (6 weeks)

Pittsburg Sleep Quality Index (PSQI)

Time Frame: Baseline, Post-intervention (6 weeks)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Prashant Kumar
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Prashant Kumar

Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation

Study Sites (1)

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